Global Variome shared LOVD
PDE6A (phosphodiesterase 6A, cGMP-specific, rod, alpha)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
Global Variome, with Curator vacancy
View all genes
View PDE6A gene homepage
View graphs about the PDE6A gene database
Create a new gene entry
View all transcripts
View all transcripts of gene PDE6A
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene PDE6A
View all variants in gene PDE6A
Full data view for gene PDE6A
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
View all individuals with variants in gene PDE6A
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene PDE6A
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene PDE6A
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
Phenotypes for disease #05611 (NDD (neurodevelopmental disorder (NDD)))
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
How to query this table
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
3690 entries on 37 pages. Showing entries 1 - 100.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
3
4
5
6
7
8
9
10
11
...
Next
Last »
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Owner
Individual ID
0000187348
severe DD/ID
-
severe developmental delay/intellectual disability; Generalized tonic-clonic seizures (onset at 5 years), nocturnal, treatment with Keppra and Micropakine; Limb hypertonia, spastic tetraparesis; normal vision, normal hearing; MRI brain enlargement of the ventricular system and peri-cerebral spaces, thin and irregular appearance of the corpus callosum; Stereotypic movements; microcephaly, plagiocephaly; Small nose, anteverted nares; normal philtrum; Wide mouth with square upper lip; Small teeth, gingival hypertrophy; Prognathism; synophrys, hypertrichosis; Hypertelorism, short neck; no mesomelic dysplasia; Bilateral elbow dislocation; Limited pronosupination, bilateral camptodactyly, edema of back-hands and -feet, bilateral simian creases, tapered fingers, dorsum pedis edema, small toes, hypoplasia of distal phalanges, ungual hypoplasia, neonatal arthrogryposis; Scoliosis; Bilateral coxa valga, dislocation of the hips; no horseshoe kidney; failure to thrive; Apnea; Bilateral cryptorchidism, bicuspid aortic valve
Isolated (sporadic)
17y
-
-
-
Johan den Dunnen
00248352
0000187349
severe DD/ID
-
severe developmental delay/intellectual disability; Multifocal epileptiform discharges in bilateral posterior quadrant, no clinical seizures.; Generalized hypotonia; Cortical visual impairment, hyperopic refractive error and small angle intermittent strabismus; MRI brain partial agenesis of the corpus callosum, forshortened and undersulcated frontal lobes, small cerebellar vermis with mega cisterna magna and wide sylvian fissures; no microcephaly; Prominent columella; normal philtrum; Wide mouth, downturned corners, thin upper lip; Small, widely spaced teeth, bruxism; normal chin; -; Full cheeks, mild facial asymmetry; mesomelic dysplasia lower limbs; Bilateral fibular agenesis, short and curved tibia, bilateral Syme amputations with resection of cartilaginous fibular anlage and bilateral tibial osteotomies for angular deformity correction, fitted with bilateral lower extremity prosthetics at 2 years 3 months.; Right single transverse and left bridged palmar crease, bilateral hypoplastic 4th metatarsals, absence of the 5th ray and phalanges of lateral toes, 4 splayed toes; 13 rib-bearing thoracic-type vertebrae and 5 lumbar type vertebrae, hypoplastic L1 with focal kyphosis; normal hips and pelvis; osteopenia; horseshoe kidney; gastroesophageal reflux disease, dysphagia, gastrostomy tube dependent, concerns for esophageal dysmotility ± abnormal gastric accommodation, abnormal gastric emptying with no evidence of small intestinal dysmotility; no failure to thrive; Multicompartmental respiratory disease (upper airway obstruction, lower airway obstruction, ineffective mucociliary clearance, restrictive lung disease, aspiration and pneumonia), moderate to severe mixed sleep apnea, severe laryngomalacia status post supraglottoplasty at 18 months, cough assist and inhaled steroid and bronchodilator and supplemental oxygen with sleep, tonsillectomy and adenoidectomy planned; History of bilateral vesicoureteral reflux, grade II
Isolated (sporadic)
03y
-
-
-
Johan den Dunnen
00248353
0000187350
severe DD/ID
-
severe developmental delay/intellectual disability; Generalized, tonic-clonic seizures (onset at 5 months), initially controlled with phenobarbital, developed drug-resistance, partially controlled with carbamazepine, clobazam, nitrazepam and phenobarbital; Axial hypotonia, peripheric hypertonia; normal vision, normal hearing; MRI brain pachygyria of frontal lobes, abnormal opercularization of insulae with thicker insular cortices, wide Sylvian fissures, cerebral atrophy, brainstem hypoplasia, increased volume of the trigones and occipital horns of the lateral ventricles; microcephaly; Large nose with bulbous nasal tip and low hanging columella; short philtrum; Wide mouth with square upper lip; teeth and gum abnormalities; Micrognathia; synophrys, hypertrichosis; mesomelic dysplasia 4 limbs; arms and legs Madelung deformity, slender limb bones, fibular hypoplasia/agenesis; Hypoplastic talipes, fusion of tarsal bones; Severe scoliosis, C2-C3 vertebral fusion, L5-S1 vertebral cleft; normal hips and pelvis; osteopenia, osteoporosis; no horseshoe kidney; gastroesophageal reflux disease, constipation; failure to thrive; Neonatal respiratory distress, recurrent pneumonia, frequent hiccups improved with carbamazepine, respiratory arrest leading to death at 21 years
Isolated (sporadic)
18y
-
-
-
Johan den Dunnen
00248354
0000187351
severe DD/ID
-
severe developmental delay/intellectual disability; Generalized, tonic-clonic seizures; Limb hypertonia; Myopia, strabismus; no microcephaly; Large nose with bulbous nasal tip and low hanging columella; short philtrum; Wide mouth with square upper lip; teeth and gum abnormalities; Triangular chin; synophrys, hypertrichosis; mesomelic dysplasia 4 limbs; Short ulna and radius, radial head dislocation/subluxation, styloid process of ulna on radius, carpal coalition, hypoplastic femora, short and curved tibia with metaphyseal flaring, mid tibial dimples, deviated knees, hypoplastic and gracile fibula; Carpal coalition, small feet, hypoplastic left 5th, metatarsal synostosis; Scoliosis; Bilateral coxa valga with hypoplastic ilia, hip dislocation; osteopenia; horseshoe kidney; gastroesophageal reflux disease, constipation; failure to thrive; no respiratory problems; Menstrual cycle perturbations
Isolated (sporadic)
21y
-
-
-
Johan den Dunnen
00248355
0000187352
severe DD/ID
-
severe developmental delay/intellectual disability; Generalized, tonic-clonic seizures; Hypotonia; Strabismus; MRI brain cerebral atrophy with possible brainstem hypoplasia; microcephaly; Small nasal tip; normal philtrum; Wide mouth with square upper lip; Small, widely spaced teeth; normal chin; synophrys, hypertrichosis; mesomelic dysplasia 4 limbs; Short and thick ulna, slightly shortened radius with convex distal end bilaterally, dislocation of right radial head, short and curved tibia, extremely short rectangular fibula; Talus ossified in hindfoot, one ossified bone in midfoot (cuneiform), missing one lateral ray in left foot, 4th-5th right metatarsal synostosis; Bilateral cervical ribs; Coxa valga; no osteopenia; horseshoe kidney; Constipation, swallowing difficulties, percutaneous endoscopic gastrostomy; failure to thrive; Nightly desaturations treated with CPAP from 3 years of age
Isolated (sporadic)
05y
-
-
-
Johan den Dunnen
00248356
0000187353
severe DD/ID
-
severe developmental delay/intellectual disability; Complex partial with secondary generalization; Axial hypotonia, peripheric hypertonia; Central vision loss due to occipital impairment, central progressive hearing loss; MRI brain prominence of CSF spaces; brachycephaly, no microcephaly; Bulbous nasal tip, low hanging columella with low insertion; short smooth philtrum; Wide mouth with downturned corners, thick lower lip vermillion; teeth and gum abnormalities; Micrognathia; synophrys, hypertrichosis; Long palpebral fissures, low-set and posteriorly rotated large ears with a simple helix, facial asymmetry; mesomelic dysplasia 4 limbs; Short fibula, discoid meniscus, limited knee extension; Soft tissue syndactyly of fingers 3rd-4th, small feet, pes planus, 2nd toe overlapping hallux bilaterally; Scoliosis, incomplete coronal cleft of T9 and T12 vertebrae, low lying spinal cord, termination of conus medullaris at upper border of L3; Bilateral coxa valga; osteopenia; horseshoe kidney; gastroesophageal reflux disease, gastrojejunostomy tube dependent, chronic constipation, hiatal hernia, pancreatitis; failure to thrive; no respiratory problems
Isolated (sporadic)
09y
-
-
-
Johan den Dunnen
00248357
0000187354
severe DD/ID
-
severe developmental delay/intellectual disability; Generalized, tonic-clonic seizures; Hypotonia; normal vision, normal hearing; MRI brain cerebral atrophy; microcephaly; Large nose with bulbous nasal tip and low hanging columella; short philtrum; Prominent upper lip; no teeth and gum abnormalities; Mild micrognathia; synophrys, hypertrichosis; Long palpebral fissures; mesomelic dysplasia 4 limbs; Limited supination, radial head dislocation/subluxation, hypoplastic fibula; Limited supination, pes planus, broad toe tips; Pectus excavatum; Hip dislocation; osteopenia, osteoporosis; no horseshoe kidney; Constipation; failure to thrive; no respiratory problems
Isolated (sporadic)
08y
-
-
-
Johan den Dunnen
00248358
0000187355
severe DD/ID
-
severe developmental delay/intellectual disability; Generalized (onset at 3 years), tonic-clonic seizures, inefficient treatments but remission since 6 years 9 months; Hypotonia; Strabismus inconstant; MRI brain cerebral atrophy, pachygyria of frontal lobes; microcephaly; Large nose with bulbous nasal tip and low hanging columella; short philtrum; Wide mouth; Widely spaced teeth; Prognathism; synophrys, hypertrichosis; Long palpebral fissures, low set ears, mild facial asymmetry, gingival hyperplasia diabetes; mesomelic dysplasia 4 limbs; Short humerus, hypoplastic short fibula; Transverse palmar crease, limited pronosupination, proximal deviation of thumbs, small feet, absent calcanei, broad 1th toes, polydactyly, cutaneous process on the side of the 5th finger and cutaneous syndactyly 3th-6th toes on left foot, four metatarsals and partial syndactyly 3th-4th toes on right foot; Scoliosis, fusion 1th-2th ribs, sacral sinus; Coxa valga, hip dysplasia; no osteopenia; horseshoe kidney; Сonstipation, anal dystopia; failure to thrive; no respiratory problems; Popliteal pterygium
Isolated (sporadic)
08y
-
-
-
Johan den Dunnen
00248359
0000187356
severe DD/ID
-
see paper; …
Isolated (sporadic)
8y
-
-
-
Johan den Dunnen
00248360
0000187357
severe DD/ID
-
severe developmental delay/intellectual disability; Generalized, tonic-clonic seizures; Hypotonia; Strabismus; microcephaly; Ankyloglossia; teeth and gum abnormalities; mesomelic dysplasia lower limbs; Bowed radii, unilateral bowed ulna, shortened ulna, abnormal radial diaphysis, bowed and angulated tibias, hypoplastic fibula; Wide distal radial metaphyses, oligodactyly: 2 tarsal bones on each foot, absent/hypoplastic calcanei, 3 metatarsals, 3 associated phalanges, 1 phalanx not associated with a metatarsal bone; Scoliosis, cervical ribs, anterior superior vertebral notching, tethered cord; Coxa valga, unilateral hip dysplasia; osteopenia; horseshoe kidney; gastroesophageal reflux disease, constipation; failure to thrive; no respiratory problems
Isolated (sporadic)
11y
-
-
-
Johan den Dunnen
00248361
0000187358
severe DD/ID
-
severe developmental delay/intellectual disability; Myoclonic jerks, convulsions; MRI brain atrophy, ventriculomegaly; dolicocephaly, no microcephaly; Short palpebral fissures, low set ears, short neck; mesomelic dysplasia 4 limbs; arms and legs radial head dislocation/subluxation, slightly short radius and ulna, short and dysplastic triangular tibias, fibular agenesis; Small equinovalgus feet, oligodactyly: 4 toes on 1 foot, 5 on the other, abnormally spaced; Sacral sinus; horseshoe kidney; Colon malrotation; failure to thrive; Recurrent apnea, 4m-respiratory arrest leading to death
Isolated (sporadic)
00y04m
-
-
-
Johan den Dunnen
00248362
0000187366
Cornelia de Lange syndrome
CHOPS
round face, hair appears thick and coarse, eyes showed long eyelashes and thick eyebrows, synophyrys; developmental delay; low lying conus with lipoma of the filum terminale; Hyperreflexia; no hearing loss; no cataract; chronic lung disease (due to recurrent aspiration?); no tracheostomy; Sleep apnea; Asthma, history of pneumonia; PDA with repair; pulmonary hypertension; Delayed gastric emptying; constipation; no gastrostomy tube; splenomegaly by abd MRI; reflux; Horseshoe kidney; brachydactyly; Abnormal shape of vertebral bodies with decreased height most pronounced from T8 to L1. ; no microcephaly; 14y-OFC 25th percentile, weight <3rd percentile, height <3rd percentile; obesity; short stature; no immunodeficiency
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00248372
0000187367
Cornelia de Lange syndrome
CHOPS
proptotic appearance to eyes, eyebrows were thick with arch and synophrys, hypertelorism, thickened helices, short nose with upturn, long philtrum, thickened tongue, high narrow palate ; developmental delay; hearing loss; no cataract; Myopia and mild optic atrophy; Subglottic stenosis (grade 2-3) and tracheomalcia, laryngomalasia; chronic lung disease; tracheostomy; Aspiration pneumonia; VSD, PDA with repair, anomalous pulmonary vein; g astrostomy tube Nissen G-tube; reflux; cryptorchidism; bilateral ureteral reflux ; brachydactyly; Congenital fusion of vertebrae C2-C3 and a history of congenital hip subluxation bilaterally. ; hypoplastic changes of L1 and L2 with anterior beaking; no microcephaly; 8y-head circumference 3rd-10th percentile, weight <3rd percentile, height <3rd percentile; obesity; short stature; history of fungal sepsis
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00248373
0000187368
Cornelia de Lange syndrome
CHOPS
round face, synorphyrys, downturn corners mouth, curly hair; developmental delay; cataract; Congenital narrow oropharyinx and laryngomalacia; chronic lung disease; no tracheostomy; Obstructive sleep apnea; PDA, PFO, and VSD; gastrostomy tube; vesico-ureteral reflux; brachydactyly appears on pictures; microcephaly; 6y-head circumference <3rd percentile, weight <3rd percentile, height <3rd percentile; obesity; short stature;
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00248374
0000187369
developmental delay
CHOPS
see paper; …, Synophrys, upturned nose, long eyelashes, microcephaly, plagiocephaly; birth weight 2,182 g (−2.27 SD), height 43 cm (−3.6 SD), head circumference 32 cm (−1.6 SD); latest weight 41.7 cm (+1.5 SD), height 120 cm (−3.5 SD), head circumferance 50 cm (−2 SD) ; VSD, PDA; Chronic respiratory issues when young‐resolved; No hearing loss; Brachydactyly, short stature treated with growth hormone treatment; no genitourinary reported; no GI reported; Hypothyroidism
Isolated (sporadic)
11y
-
-
-
Johan den Dunnen
00248375
0000187370
developmental delay
CHOPS
see paper; …, Synophrys, upturned nose, downslanting palpebral fissures, prominent vertical forehead crease, large anterior fontanelle, thick cranial vault with prominent Wormian bones along the lambdoid suture, microbrachycephaly; birth weight 3,430 g (−0.18 SD), height 48 cm (−0.75 SD), head circumference 34.5 cm (0 SD); latest weight 84.8 kg (+0.98 SD), height 142.7 cm (−4.6 SD), head circumferance 58 cm (+2 SD) ; None reported; Noisy breather and snores but not significant apnea; Mild sensorineural hearing loss; Brachydactyly, joint hypermobility (Beighton score 6/9), mild truncal hypotonia, osteopenic bones, immature ovoid appearance to the vertebral bodies of the thoracic and lumbar spine, narrowing of the T11/12 intervertebral disc space, mild shortening of the proximal humeri and metacarpals, hypoplasia of the distal phalanges of the toes, pes planus, limited extension of the right elbow, small hands and feet; Horseshoe kidney, mild coronal hypospadias (repaired), small genitalia; no GI reported; Strabismus, bilateral ptosis, gynecomastia, acanthosis nigricans, hirsutism
Isolated (sporadic)
23y
-
-
-
Johan den Dunnen
00248376
0000187371
developmental delay
CHOPS
see paper; …, Mild Synophrys with prominent eyebrows, prominent eyelashes, bilateral proptosis, facial hirsutism, upturned nose, bitemporal narrowing, microcephaly, cupped ears with simple helices, high arched palate, and clubbing of nails, hands and feet; birth weight 1,474 (−3.34 SD), height 38 cm (−6.17 SD); latest weight 20.9 kg (−2 SD), height 93.8 cm (−5.9 SD), head circumferance 47 cm (−4.1 SD) ; VSD, congenital dilated aortic root, pulmonary hypertension; Subglottic stenosis, chronic lung disease and respiratory failure, tracheostomy, idiopathic pulmonary hemosiderosis, diffuse pulmonary alveolar hemorrhage, acute interstitial pneumonia; Bilateral sensorineural hearing loss; Absent left thumb (not congenital); Single kidney, sexual precocity; Nissen‐G tube, constipation, GERD; Astigmatism, otorrhea, optic nerve hypoplasia of left eye, intermittent exotropia, ptosis, chronic bilateral otitis media, hyperglycemia, polycythemia, steroid‐induced diabetes mellitus, iatrogenic adrenal insufficiency, prematurity
Isolated (sporadic)
09y
-
-
-
Johan den Dunnen
00248377
0000187372
developmental delay
CHOPS
see paper; …, Synophrys, trace proptosis, small upturned nose with shallow bridge, prominent cheeks, macroglossia, micrognathia, bitemporal narrowing, and microcephaly; birth weight 2,239 g (−2.18 SD), height 43 cm (−2.98 SD), head circumference 29.5 cm (−3.7SD); latest weight 10.82 kg (−1.1 SD), height 73 cm (−4.1 SD), head circumferance 43.5 cm (−2.8 SD) ; PDA, PFO, dilated aortic root; History of pneumonia, chronic lung disease, chronic congestion and noisy breathing, acute chronic respiratory failure, subglottic narrowing of trachea; Mild conductive hearing loss; Disharmonic skeletal maturation of the hands; no genitourinary reported; G tube, dysphagia; Obstruction of nasolacrimal duct, chronic bilateral otitis media, sacral mass (removed), jaundice
Isolated (sporadic)
02y
-
-
-
Johan den Dunnen
00248378
0000187373
developmental delay
CHOPS
see paper; …, Synophrys, coarse appearance to features; birth weight 2,070 g (−1.5 SD), height 43 cm (−1.9 SD), head circumference 29 cm (−3.23 SD); latest weight 10th centile, height 90 cm (−6.1SD), head circumferance 3rd centile; None reported; History of aspirations; Mixed hearing loss; Brachydactyly; no genitourinary reported; no GI reported; Mild myopia with strabismus, skin changes (sun exposed erythema and mottling of his skin)
Isolated (sporadic)
07y
-
-
-
Johan den Dunnen
00248379
0000187374
developmental delay
CHOPS
see paper; …, Round face, brachiocephaly, microcephaly, long eyelashes, high arch eyebrows/curved, broad ICD, ears cupped and somewhat simplified; birth weight 1,170 g (−3.13 SD); latest weight 17.3 kg (−1.5 SD), height 88 cm (−5.7 SD), head circumferance 48 cm (−2.6 SD) ; PDA, PFO; Chronic lung disease due to apnea and aspirations, tracheostomy; Bilateral sensorineural hearing loss (improved); None reported; no genitourinary reported; G tube; Cataract, myopia, amblyopia, exophoria, growth hormone deficiency
Isolated (sporadic)
06y
-
-
-
Johan den Dunnen
00248380
0000187375
developmental delay
CHOPS
see paper; …, Round face, synophrys, downturn corners of the mouth, curly hair, long eyelashes and thick eyebrows; birth weight 2,570 g (−1.1 SD), height 50 cm (+0.8 SD), head circumference 33 cm (+0.1 SD); latest weight 16 kg (−2.1 SD), height 98.5 cm (−4.7SD), head circumferance 47.6 cm (−1.9 SD) ; VSD; None reported; Bilateral conductive hearing loss; Brachydactyly; no genitourinary reported; G tube; Cataract, low lying conus with lipoma of the filum terminale
Isolated (sporadic)
07y
-
-
-
Johan den Dunnen
00248381
0000187376
developmental delay
CHOPS
see paper; …, Round face, arched eyebrows, long philtrum, thin upper lip, low‐set posteriorly rotated ears; birth weight 1,560 g (−4.6SD, height 39 cm (−5.8 SD), head circumference 29 cm (−4.3 SD); latest weight 8.6 kg (−1.1 SD), height 66 cm (−4.1 SD), head circumferance 42 cm (−3.2 SD); None reported; Episodes of pneumonia and upper respiratory infection; Mixed bilateral hearing loss; Brachydactyly; small hands and feet, left fifth finger clinodactyly, single crease on left fifth finger, abnormal shape of vertebral bones, short iliac bones, small left femoral head; Short prepuce; History of constipation
Isolated (sporadic)
01y
-
-
-
Johan den Dunnen
00248382
0000187377
Cornelia de Lange syndrome
CHOPS
see paper; ..., Synophrys, upturned nose, long philtrum, thick arched eyebrows, long eyelashes, large anterior fontanelle, microcephaly, microbrachycephaly, Wormian bones on her skull; birth weight 2,381 g (−1.94 SD), head circumference 31.1 cm (−2.3 SD); latest weight 32.9 kg (−3.7 SD), height 118.1 cm (−6.9 SD), head circumferance 53 cm (25th centile) 14y; PDA, chronic right‐sided heart failure, pulmonary hypertension; Chronic lung disease of uncertain etiology (status post ARDS) and low oxygen saturations, sleep apnea, asthma, history of aspiration and pneumonia; No hearing loss; Brachydactyly, small hands with proximally placed thumbs, abnormal shape of vertebral bodies with decreased height most pronounced from T8 to L1; Horseshoe kidney with repeated episodes of acute kidney injury, chronic kidney disease, diuretic‐associated metabolic alkalosis and hypokalemia; Vomiting and dehydration with delayed gastric emptying, constipation, Candida esophagitis, GERD; Coarse hair
Isolated (sporadic)
20y
-
-
-
Johan den Dunnen
00248372
0000187379
Cornelia de Lange syndrome
CHOPS
see paper; ..., Synophrys, upturned nose, arched eyebrows, thick ears posteriorly rotated; birth weight 1,757 g (−2.94 SD), height 43 cm (−2.98 SD); latest weight 15.6 kg (−2.1 SD) 6y, height 83.7 cm (−7.3 SD) 6y, head circumferance −3 SD 6y ; PDA, PFO, VSD; Congenital narrow oropharynx, laryngomalacia, chronic lung disease, RAD, tracheostomy, obstructive sleep apnea; No hearing loss; Brachydactyly, deformity and hypoplasia of the proximal radius and fibula bilaterally, focal lumbar kyphoscoliosis at the thoracolumbar junction; Mild grade I vesicoureteral reflux; G tube, constipation; Bilateral cataracts, eczema
Isolated (sporadic)
12y
-
-
-
Johan den Dunnen
00248374
0000199315
neurodevelopmental syndrome
-
see paper; …, mild
Isolated (sporadic)
17y
-
-
-
Johan den Dunnen
00260784
0000199316
neurodevelopmental syndrome
-
see paper; …, mild
Isolated (sporadic)
13y
-
-
-
Johan den Dunnen
00260785
0000199317
neurodevelopmental syndrome
-
see paper; …, mild
Isolated (sporadic)
3y
-
-
-
Johan den Dunnen
00260786
0000199318
neurodevelopmental syndrome
-
see paper; …, mild
Isolated (sporadic)
4y
-
-
-
Johan den Dunnen
00260787
0000199319
neurodevelopmental syndrome
-
see paper; …, mild
Isolated (sporadic)
7y
-
-
-
Johan den Dunnen
00260788
0000199320
neurodevelopmental syndrome
-
see paper; …, mild
Isolated (sporadic)
7y
-
-
-
Johan den Dunnen
00260789
0000199321
neurodevelopmental syndrome
-
see paper; …, mild
Isolated (sporadic)
9y
-
-
-
Johan den Dunnen
00260790
0000199322
neurodevelopmental syndrome
-
see paper; …, moderate
Isolated (sporadic)
11y
-
-
-
Johan den Dunnen
00260791
0000199323
neurodevelopmental syndrome
-
see paper; …, moderate
Isolated (sporadic)
6y
-
-
-
Johan den Dunnen
00260792
0000199324
neurodevelopmental syndrome
-
see paper; …, moderate
Isolated (sporadic)
13y
-
-
-
Johan den Dunnen
00260793
0000199325
neurodevelopmental syndrome
-
see paper; …, moderate
Isolated (sporadic)
7y
-
-
-
Johan den Dunnen
00260794
0000199326
neurodevelopmental syndrome
-
see paper; …, severe
Isolated (sporadic)
18y
-
-
-
Johan den Dunnen
00260795
0000199327
neurodevelopmental syndrome
-
see paper; …, severe
Isolated (sporadic)
6y
-
-
-
Johan den Dunnen
00260796
0000199328
neurodevelopmental syndrome
-
see paper; …, severe
Isolated (sporadic)
4y
-
-
-
Johan den Dunnen
00260797
0000199329
neurodevelopmental syndrome
-
see paper; …, profound
Isolated (sporadic)
9y
-
-
-
Johan den Dunnen
00260798
0000199330
neurodevelopmental syndrome
-
see paper; …
Isolated (sporadic)
<0d
-
-
-
Johan den Dunnen
00260799
0000199340
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
20y
-
-
-
Johan den Dunnen
00260807
0000199341
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
1y9m
-
-
-
Johan den Dunnen
00260808
0000199342
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
14y
-
-
-
Johan den Dunnen
00260809
0000199343
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
5y8m
-
-
-
Johan den Dunnen
00260810
0000199344
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
3y6m
-
-
-
Johan den Dunnen
00260811
0000199345
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
12y
-
-
-
Johan den Dunnen
00260812
0000199346
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
6y
-
-
-
Johan den Dunnen
00260813
0000199347
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
6y
-
-
-
Johan den Dunnen
00260814
0000199348
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
15y
-
-
-
Johan den Dunnen
00260815
0000199349
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
4y
-
-
-
Johan den Dunnen
00260816
0000199350
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
5y3m
-
-
-
Johan den Dunnen
00260817
0000199351
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
10y
-
-
-
Johan den Dunnen
00260818
0000199352
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
24y
-
-
-
Johan den Dunnen
00260819
0000199353
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
41y
-
-
-
Johan den Dunnen
00260820
0000199354
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
13m
-
-
-
Johan den Dunnen
00260821
0000199355
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
7y9m
-
-
-
Johan den Dunnen
00260822
0000199356
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
12y
-
-
-
Johan den Dunnen
00260823
0000199357
neurodevelopmental disorder
-
see paper; …
Familial, autosomal dominant
2y2m
-
-
-
Johan den Dunnen
00260824
0000199358
neurodevelopmental disorder
-
see paper; …
Isolated (sporadic)
30y
-
-
-
Johan den Dunnen
00260825
0000203961
intellectual disability
-
short stature (146cm), head circumference 51cm (<1 percentile); severe intellectual disability, developmental delay; aphasia; delayed motor milestones; no epilepsy; (mild) hypotonia; behaviour aggressive; low vision
Familial, autosomal recessive
36y
-
-
-
Johan den Dunnen
00266184
0000203962
intellectual disability
-
short stature (150cm), head circumference 51cm (<1 percentile); severe intellectual disability, developmental delay; aphasia; delayed motor milestones; no epilepsy; (mild) hypotonia; behaviour aggressive; lower limbs weakness
Familial, autosomal recessive
23y
-
-
-
Johan den Dunnen
00266185
0000203963
intellectual disability
-
short stature (120cm), head circumference 48cm (25th percentile); severe intellectual disability, developmental delay; speech few words; delayed motor milestones; (early on-set) epilepsy; hypotonia; behaviour inattention and hyperactivity; MRI normal; multiple hyperpigmented café au lait spots in his lower back and upper thigh, truncal ataxia and ataxic gait with frequent falls
Familial, autosomal recessive
6y
-
-
-
Johan den Dunnen
00266186
0000203964
intellectual disability
-
short stature (148cm), head circumference 53cm (50th percentile); severe intellectual disability, developmental delay; speech few words; delayed motor milestones; (early on-set) epilepsy; hypotonia; behaviour aggressive, ADHD and hyperactivity; MRI normal; unsteady gait
Familial, autosomal recessive
11y
-
-
-
Johan den Dunnen
00266187
0000203965
intellectual disability
-
short stature (119cm), head circumference 49cm (25th percentile); severe intellectual disability, developmental delay; speech few words; delayed motor milestones; (early on-set) epilepsy; hypotonia; behaviour inattention and hyperactivity; MRI normal; unsteady gait
Familial, autosomal recessive
6y
-
-
-
Johan den Dunnen
00266188
0000207605
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; autistic features/stereotypy; hyperactivity; screaming/laughing spells; self-injury/hand-biting; bruxism; hypotonia in infancy; nonambulatory; no seizures; microcephaly; secondary microcephaly; no dysmorphic features; no ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
10y
-
-
-
Caroline Dias
00269814
0000207606
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; autistic features/stereotypy; hyperactivity; screaming/laughing spells; self-injury/hand-biting; bruxism; hypotonia in infancy; nonambulatory; no seizures; microcephaly; no dysmorphic features; no ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
16y
-
-
-
Caroline Dias
00269815
0000207607
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; autistic features/stereotypy; hyperactivity; screaming/laughing spells; self-injury/hand-biting; bruxism; hypotonia in infancy; nonambulatory; no seizures; microcephaly; secondary microcephaly; no dysmorphic features; no ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
9y
-
-
-
Caroline Dias
00269816
0000207608
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; autistic features/stereotypy; no hyperactivity; screaming/laughing spells; no self-injury/hand-biting; no bruxism; hypotonia in infancy; nonambulatory; MRI brain abnormalities; no seizures; no microcephaly; dysmorphic features; ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
11y
-
-
-
Caroline Dias
00269817
0000207609
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; no autistic features/stereotypy; hyperactivity; screaming/laughing spells; self-injury/hand-biting; no bruxism; hypotonia in infancy; nonambulatory; seizures; no dysmorphic features; no ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
21y
-
-
-
Caroline Dias
00269818
0000207610
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; no hyperactivity; -; hypotonia in infancy; no seizures; no microcephaly; dysmorphic features; no ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
1y4m
-
-
-
Caroline Dias
00269819
0000207611
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; autistic features/stereotypy; no hyperactivity; screaming/laughing spells; -; bruxism; hypotonia in infancy; nonambulatory; MRI brain abnormalities; no seizures; microcephaly; dysmorphic features; ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
9y
-
-
-
Caroline Dias
00269820
0000207612
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; autistic features/stereotypy; no hyperactivity; no screaming/laughing spells; -; bruxism; hypotonia in infancy; nonambulatory; MRI brain abnormalities; no seizures; no microcephaly; dysmorphic features; ophthalmologic features; gastrointestinal symptoms
Familial, autosomal recessive
5y
-
-
-
Caroline Dias
00269821
0000207613
neurodevelopmental delay
-
intellectual disability/global developmental delay; motor delay; language delay; no autistic features/stereotypy; hyperactivity; no screaming/laughing spells; no self-injury/hand-biting; no bruxism; no hypotonia in infancy; ambulatory; MRI brain abnormalities; no seizures; no microcephaly; dysmorphic features; no ophthalmologic features; no gastrointestinal symptoms
Familial, autosomal recessive
8y
-
-
-
Caroline Dias
00269822
0000210490
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-1y10m; fine motor delay; first words-24m; speech three word sentences; received speech/language therapy; initially dfficulties with repeating words, good understanding; can now very well communicate his wishes; developmental delay; autistic features; no ADHD/ADD; open towards others, sometimes difficult behaviour with temper tantrums in stress, hand-flapping; normal weight; normal height; macrocephaly; MRI-brain normal; no wide CSF spaces; hypotonia; no epilepsy, no seizures; poor in motion transitions. Inward rotation of the feet when walking, slightly broad based; high forehead with frontal bossing; widely spaced eyes; normal teeth; high arched palate; no neonatal issues; normal vision; normal hearing; normal heart; orchidopexia performed; Hyperlaxity of all major joints; loves to eat, needs to be controlled by parents, intermittend hyperphosphatesia,
Isolated (sporadic)
3y7m
-
-
-
Johan den Dunnen
00275891
0000210491
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y7m; fine motor delay; speech babbles only, uses some signs; received speech/language therapy; babbles only, some signs,receptive language is strong: knows letters, numbers, shapes, colors, has some sign language; developmental delay, probably normal intelligence with speech delay; no autism/autistic features; no ADHD/ADD; Happy, social, engaged with others. Affectionate, friendly, described as endearing. Good disposition. Sensory issues to loud noise, bright lights, swings; normal weight; normal height; macrocephaly; MRI-brain thin corpus callosum; no wide CSF spaces; hypotonia; no epilepsy, no seizures; broad based gait with arms flexed. slight external rotation of both lower extremities; high forehead with frontal bossing; no widely spaced eyes; normal teeth; high arched palate; one neonatal episode of hypoglycemia; hypermetropia; normal hearing; normal heart; normal kidneys; no male genital abnormalities; no hernias; Hypotonia in legs; Brown syndrome, laryngeal cleft, patch of tan discloration of skin on back of neck and mid-back, obstructive sleep apnea
Isolated (sporadic)
3y
-
-
-
Johan den Dunnen
00275892
0000210492
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y6m; fine motor delay; first words-1y6m; speech complete sentences; received speech/language therapy; speech/language delay; Borderline intellectual disability (verbal IQ 87, performance IQ 78); no autism/autistic features; attention deficit without hyperactivity; No other behavioral problems; normal weight; normal height; no macrocephaly, no microcephaly; MRI-brain normal; no wide CSF spaces; hypotonia; no epilepsy, no seizures; dystonia, broad based gait; prominent forehead with frontal bossing; widely spaced eyes; teeth malposition; high arched palate; no neonatal issues; convergent strabism, astigmatism, hypermetropia; hyperacusis; normal heart; normal kidneys; no hernias; Joint hyperlaxity, adducted thumbs; pneumonitis, pyelonephritis
Isolated (sporadic)
4y
-
-
-
Johan den Dunnen
00275893
0000210493
neurodevelopmental delay
SNIBCPS
global developmental delay; no walking yet; fine motor delay; first words-1y6m; speech 3-4 words; received speech/language therapy; expressive speech delay. Receptive speech appears normal; developmental delay; no autism/autistic features; bruxism; normal weight; normal height; no macrocephaly, no microcephaly; MRI-brain subgaleal hematoma, no other abnormalities; no wide CSF spaces; hypotonia; no epilepsy, no seizures; normal; normal forehead; widely spaced eyes; missing maxillary lateral incisors; normal palate; neonatal cephalohematoma; congenital entropion; conductive hearing loss; normal heart; normal kidneys; left testis initially undescended, now retractile. webbing between penis and scrotum; no hernias; no skeletal anomalies, no joint anomalies; Sleep apnea. non-pitting edema in feet
Isolated (sporadic)
2y3m
-
-
-
Johan den Dunnen
00275894
0000210494
neurodevelopmental delay
SNIBCPS
global developmental delay; no walking yet; fine motor delay; no speech; did not receive speech/language therapy; no speech; severe intellectual disability; no autism/autistic features; no ADHD/ADD; always pleasant in behaviour; weight <-2.5 SD; height <-2.5 SD; microcephaly; MRI-brain normal (except for microcephaly); no wide CSF spaces; hypotonia; no epilepsy, no seizures; spastic tetraplegia; sloping forehead; widely spaced eyes; large teeth; normal palate; neonatal feeding problems, PEG tube; normal vision; normal hearing; normal heart; normal kidneys; no hernias; severe orthopedic problems hip, feet. Luxations of thumbs, wrists, shoulders on young age, not anymore; unilateral choane atresia + hypoplastic epilglottis. Siallorhea requiring botox and radiotherapy.
Isolated (sporadic)
15y
-
-
-
Johan den Dunnen
00275895
0000210495
neurodevelopmental delay
SNIBCPS
global developmental delay; fine motor delay; first words-2y; speech complete sentences; received speech/language therapy; language production and reception impaired; Mild intellectual disability (IQ 58); PDD-NOS; no ADHD/ADD; Flapping, hyperactive and claiming behaviour. Stereotypic movements; normal weight; normal height; no macrocephaly, no microcephaly; MRI-brain widening of CSF spaces; wide CSF spaces; hypotonia; neonatal convulsions; abnormal gait; broad forehead, frontal bossing; widely spaced eyes; taurodontia, delayed changing into adult dentition; normal palate; neonatal feeding problems; cerebral visual impairment, nystagmus, strabism, hypermetropia; normal hearing; normal heart; normal kidneys; no hernias; joint hyperlaxity; drooling until 8y, high pain treshold, sleeping problems. V-shaped sacral crease
Isolated (sporadic)
11y
-
-
-
Johan den Dunnen
00275896
0000210496
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-3y; fine motor delay; first words-4y; speech impaired intelligibility, high pitched voice; not known; intellectual disability (level unknown); mild autistic features; normal weight; normal height; macrocephaly; no epilepsy, no seizures; no; prominent forehead; widely spaced eyes; high arched and narrow palate; no neonatal issues; hypermetropia; normal hearing; normal heart;;
Isolated (sporadic)
17y
-
-
-
Johan den Dunnen
00275897
0000210497
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y; fine motor delay; first words-3-4y; not known; Mild intellectual disability (IQ 62); mild autistic features; normal weight; normal height; macrocephaly; MRI-brain normal; no wide CSF spaces; no epilepsy, no seizures; no; prominent forehead; no widely spaced eyes; high arched and narrow palate; no neonatal issues; hypermetropia; normal hearing; normal heart;;
Isolated (sporadic)
21y
-
-
-
Johan den Dunnen
00275898
0000210498
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-1y10m; fine motor delay; first words-1y2m; speech sentences; received speech/language therapy; no formal diagnosis besides globally delayed, sentences are mostly intelligible; developmental delay; no autism/autistic features; no ADHD/ADD; No major behavior problems, sometimes struggles with emotions and gets upset/frustrated; normal weight; normal height; macrocephaly; MRI-brain cortical abnormalities suggestive for cortical dysgenesis, mildly widened CSF spaces; wide CSF spaces; hypotonia; no epilepsy, no seizures; no; broad forehead; no widely spaced eyes; normal teeth; normal palate; no neonatal issues; normal vision; normal hearing; normal heart; normal kidneys; no hernias; hyperlaxity in elbows, ankles, and knees; One café au lait spot
Isolated (sporadic)
6y7m
-
-
-
Johan den Dunnen
00275899
0000210499
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-3y6m; speech 10 words; moderate intellectual disability; normal weight; normal height; macrocephaly; no wide CSF spaces; no epilepsy, no seizures; irregular broad based gait; prominent forehead; widely spaced eyes; no neonatal issues; normal heart;;
Isolated (sporadic)
5y
-
-
-
Johan den Dunnen
00275900
0000210500
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-1y6m; first words-4y; normal language development; moderate intellectual disability; no autism/autistic features; no ADHD/ADD; no particular behavioral problems; normal height; no macrocephaly, no microcephaly; MRI-brain normal; no wide CSF spaces; no epilepsy, no seizures; no; conical left upper incisor; no neonatal issues; hypermetropia; normal hearing; normal heart;;
Isolated (sporadic)
8y3m
-
-
-
Johan den Dunnen
00275901
0000210501
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y; fine motor delay; first words-2y; speech sentences; received speech/language therapy; Issues with speech enunciation, hypernasal voice, occasional stuttering. Impaired language on all subcompoinents of CELF4; Moderate intellectual disability; autistic features; no ADHD/ADD; Frequently puts objects in her mouth. Easily distractable and constantly needs to keep her hands busy and mind busy. Some hand-flapping and hopping on both feet, when excited; normal weight; normal height; macrocephaly; MRI-brain mildly widened CSF spaces; wide CSF spaces; hypotonia; no epilepsy, no seizures; Issues with balance, coordination; prominent forehead; widely spaced eyes; Crowded teeth - extensive dental history, instance of no permanent teeth under a decidious tooth; high arched palate with bifid uvula; caesarian section for fetal decelerations and oligohydramnios; myopia, astigmatism, strabism; normal hearing; normal heart; normal kidneys; no hernias; hyperlordosis of lumbar spine. Hypermobile flat feet; anteriorly placed anus, chronic and recurrent upper respiratory infections; increased subcutaneous adipose tissue deposition, copious saliva production evident from birth onwards, possible impairment of thirst; low hematocrit in childhood with normal hemoglobin level and MCV
Isolated (sporadic)
18y
-
-
-
Johan den Dunnen
00275902
0000210502
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y; speech sentences; severe delay, yet verbal skills scored as relative strength; Mild intellectual disability; no autism/autistic features; no ADHD/ADD; normal weight; normal height; macrocephaly; MRI-brain encephalomalacia left temporal and parietal lobes; no wide CSF spaces; no epilepsy, no seizures; Parkinsonism since 1-2 years, resting/pill-rolling tremor, progressive weakness, swallowing difficulties, long standing equinovarus posturing of one foot; tall forehead; no widely spaced eyes; normal palate; normal vision; normal heart; normal kidneys; no male genital abnormalities; no hernias; equinovarus and high arched foot (only left); Recently volvulus with colonic ischemia. Ptosis.
Isolated (sporadic)
59y
-
-
-
Johan den Dunnen
00275903
0000210503
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-1y2m; fine motor delay; first words-2y8m; speech short sentences; received speech/language therapy; Receptive language better than speech production; Severe intellectual disability; no autism/autistic features; no ADHD/ADD; always pleasant in behaviour; normal weight; normal height; no macrocephaly, no microcephaly; MRI-brain thin corpus callosum; no hypotonia; no epilepsy, no seizures; mild unsteady gait; high forehead; widely spaced eyes; normal teeth; normal palate; no neonatal issues; normal vision; normal hearing; normal heart; normal kidneys; no male genital abnormalities; no hernias; no skeletal anomalies, no joint anomalies;
Isolated (sporadic)
8y6m
-
-
-
Johan den Dunnen
00275904
0000210504
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-1y6m; fine motor delay; Speech delay; Mild intellectual disability; normal weight; normal height; MRI-brain normal; no wide CSF spaces; no epilepsy, no seizures; not known; underbite; normal vision; aortic dilatation; undescended testes, orchidopexy performed; primary hypogonadism, malar hypoplasia. Also de novo mutation in CIC gene: NM_015125.3:c.1444G>T; p.(Glu482*)
Isolated (sporadic)
14y4m
-
-
-
Johan den Dunnen
00275905
0000210505
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-5y; fine motor delay; first words-4y; speech 20 single words; received speech/language therapy; Speech and language delay, particularly expressive; severe intellectual disability; no autism/autistic features; no ADHD/ADD; no behavioral abnormalities, sociable; normal weight; normal height; macrocephaly; MRI-brain normal; no wide CSF spaces; no hypotonia; no epilepsy, no seizures; no; broad forehead; widely spaced eyes; normal teeth; submucous cleft palate; neonatal stridor, jaundice, feeding problems; hypermetropia; ear tubes; normal heart; normal kidneys; no hernias; Pes planus and laxiity of large joints; V-shaped sacral crease
Isolated (sporadic)
10y
-
-
-
Johan den Dunnen
00275906
0000210506
neurodevelopmental delay
SNIBCPS
global developmental delay; no walking yet; fine motor delay; no first words yet; no speech; did not receive speech/language therapy; Has not started speaking yet, uses melodic vocalization; Moderate intellectual disability; no autism/autistic features; no ADHD/ADD; Very attentive, pleasant social behaviour. Since age 8m recurrent oculogyral crisis and episodes of sudden movement (thrusting upward of the thorax). Also recurrent "shuddering" when emotional; normal weight; normal height; no macrocephaly, no microcephaly; MRI-brain widening of CSF spaces, bilateral cerebral atrophy, bifrontal hygromas; wide CSF spaces; hypotonia; pathological EEG at age 8m, recent EEG unremarkable (without therapy); episodes of spontaneous movement (before truncal upthrust and oculogyral crisis, now emotional head "shuddering"; frontal bossing; widely spaced eyes; normal teeth; normal palate; neonatal respiratory distress after RSV infection, ICU for 2d; normal vision; normal hearing; normal heart; normal kidneys; no male genital abnormalities; no hernias; no skeletal anomalies, no joint anomalies; multiple skin creases on left posterior thigh
Isolated (sporadic)
12m
-
-
-
Johan den Dunnen
00275907
0000210507
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-3y6m; fine motor delay; first words-1y3m-1y11m; speech repetitive and echolalic; received speech/language therapy; Moderate intellectual disability (IQ 43); no autism/autistic features; no ADHD/ADD; Some OCD-like behavior, some nervous mannerisms, routine oriented; normal weight; normal height; macrocephaly; no hypotonia; no epilepsy, no seizures; Somewhat wide-based, unsteady gait and feet slightly turned in while walking; normal forehead; no widely spaced eyes; normal teeth; normal palate; no neonatal issues; hypermetropia, amblyopia; normal hearing; normal heart; normal kidneys; no hernias; Mild scoliosis, thoracic kyphosis, and somewhat exaggerated lumbar lordosis. Mild cubitus valgus of upper extremities; Some dysfunctional uterine bleeding.
Isolated (sporadic)
21y
-
-
-
Johan den Dunnen
00275908
0000210508
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-4y; fine motor delay; first words-7y; speech only a few words; received speech/language therapy; severe language disorder (expressive and receptive); Severe intellectual disability; no autism/autistic features; timid; normal weight; normal height; macrocephaly; MRI-brain normal; no wide CSF spaces; hypotonia; no epilepsy, no seizures; no; prominent forehead; widely spaced eyes; normal teeth; high palate; neonatal respiratory distress, feeding problems; vision refractive error; ear tubes; normal heart; normal kidneys; no hernias; pectus chest deformity, joint hypermobility,; hypertrichosis
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00275909
0000210509
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-4y; fine motor delay; first words-4y; speech short sentences, hoarse voice; received speech/language therapy; Severe intellectual disability; no autism/autistic features; no ADHD/ADD; pleasant in behaviour; normal weight; normal height; no macrocephaly, no microcephaly; MRI-brain widening of CSF spaces; wide CSF spaces; hypotonia; no epilepsy, no seizures; delayed visual maturation; prominent forehead; widely spaced eyes; normal teeth; normal palate; no neonatal issues; hypermetropia, strabism, cerebral visual impairment; normal hearing; Atrial septal defect, Pulmonic valve stenosis; normal kidneys; no hernias; no skeletal anomalies, no joint anomalies;
Isolated (sporadic)
9y6m
-
-
-
Johan den Dunnen
00275910
0000210510
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-4y; fine motor delay; first words-5y; speech short sentences, hoarse voice; received speech/language therapy; Severe intellectual disability; no autism/autistic features; no ADHD/ADD; pleasant in behaviour; normal weight; normal height; no macrocephaly, no microcephaly; MRI-brain widening of CSF spaces; wide CSF spaces; hypotonia; no epilepsy, no seizures; delayed visual maturation; high forehead; widely spaced eyes; normal teeth; normal palate; no neonatal issues; hypermetropia, strabism, cerebral visual impairment; normal hearing; normal heart; normal kidneys; no hernias; no skeletal anomalies, no joint anomalies; Sagittal craniosynostosis, constipation
Isolated (sporadic)
9y6m
-
-
-
Johan den Dunnen
00275911
0000210511
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y6m; fine motor delay; first words-4y; speech sentences; received speech/language therapy; severe verbal apraxia; moderate oral apraxia; moderate receptive and expressive language disorder; mild stuttering disorder. Impaired intelligibility; Borderline intellectual disability (total IQ 72); no autism/autistic features; ADD; very sociable, hyperactive; normal weight; normal height; macrocephaly; MRI-brain normal; no wide CSF spaces; hypotonia; no epilepsy, no seizures; no; tall and boxy forehead with dimpling; widely spaced eyes; normal teeth; narrow palate; small oral cavity; no neonatal issues; normal vision, wears glasses; ear tubes; normal heart; normal kidneys; Undescended testes; inguinal hernia; no skeletal anomalies, no joint anomalies; 3 cafe au lait spots. Thin and concave toenails. Thin fingernails. Lateral right-side hair whorl. Skin syndactyly of toes (2-3).
Isolated (sporadic)
17y
-
-
-
Johan den Dunnen
00275912
0000210512
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y; fine motor delay; no first words yet; speech no words currently, vowel sounds/babbling; received speech/language therapy; Expressive language more impaired than expressive language, can follow simple instructions; developmental delay; no autism/autistic features; no ADHD/ADD; very happy, social personality; normal weight; normal height; macrocephaly; MRI-brain mildly widened CSF spaces; wide CSF spaces; hypotonia; no epilepsy, no seizures; no; high forehead with frontal bossing; widely spaced eyes; enamel hypoplasia; normal palate; neonatal respiratory distress, had to be resuscitated, in NICU for 2d; vision slight refractive error, exotropia; normal hearing; normal heart; normal kidneys; Undescended testes, hypospadias,"hidden penis"; inguinal hernia; joint hyperlaxity, wears ankle foot orthoses; abnormal bladder shape on MRI
Isolated (sporadic)
2y8m
-
-
-
Johan den Dunnen
00275913
0000210513
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-2y6m; fine motor delay; speech sentences, often not accurately constructed; received speech/language therapy; delayed speech/language development, formal diagnosis not known; developmental delay; autistic features; active, difficulty to gain attention; normal weight; normal height; no macrocephaly, no microcephaly; no wide CSF spaces; no hypotonia; no epilepsy, no seizures; no; frontal bossing; normal teeth; normal palate; neonatal feeding problems; normal vision; normal hearing; normal heart; normal kidneys; no male genital abnormalities; ingunial hernia; no skeletal anomalies, no joint anomalies;
Isolated (sporadic)
4y5m
-
-
-
Johan den Dunnen
00275914
0000210514
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-4y; fine motor delay; first words-4y; speech sentences; received speech/language therapy; speech difficulties; mild intellectual disability; no autism/autistic features; short attention span; very sociable, friendly; normal weight; normal height; macrocephaly; MRI-brain normal; no wide CSF spaces; hypotonia; no epilepsy, no seizures; no; high forehead; widely spaced eyes; normal teeth; high palate; neonatal respiratory distress and feeding problems; exophoria; normal hearing; normal heart; normal kidneys; no hernias; joint hyperlaxity; livedo
Isolated (sporadic)
10y
-
-
-
Johan den Dunnen
00275915
0000210515
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-4y; fine motor delay; no first words yet; speech single word vocalizations, signs and a communication device; received speech/language therapy; predominantly vocalizations and some word approximations. Uses communication device; Moderate intellectual disability; repetitive behaviors, hand flapping, head banging; normal weight; normal height; macrocephaly; MRI-brain mildly widened CSF spaces, mildly prominent perivascular spaces in periatrial white matter; wide CSF spaces; hypotonia; no epilepsy, no seizures; poor balance,; high forehead and minimal frontal bossing; no widely spaced eyes; upper central diastema; normal palate; no neonatal issues; has glasses; normal hearing; normal heart; both testes descended, but left testes high in scrotal sac; hiatal hernia; no skeletal anomalies, no joint anomalies; minor pigment variation and eczema. history of reactive airway disease/asthma. Reflux and esophagitis.
Isolated (sporadic)
4y7m
-
-
-
Johan den Dunnen
00275916
0000210516
neurodevelopmental delay
SNIBCPS
global developmental delay; walk-1y8m; fine motor delay; first words-13m; speech short sentences; received speech/language therapy; No specific speech or language problems; Mild-Moderate intellectual disability; no autism/autistic features; short attention span; friendly, good social behaviour; normal weight; height >+2.5 SD; macrocephaly; hypotonia; no epilepsy, no seizures; no; prominent forehead; widely spaced eyes; normal teeth; arched palate; no neonatal issues; strabism; normal hearing; normal heart; normal kidneys; no male genital abnormalities; umbilical hernia (neonatal period); no skeletal anomalies, no joint anomalies; wide mamillary distance, increased sweating
Isolated (sporadic)
3y6m
-
-
-
Johan den Dunnen
00275917
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
3
4
5
6
7
8
9
10
11
...
Next
Last »
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators