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Phenotypes for disease #00841 (EIEE (encephalopathy, epileptic, early infantile (EIEE)))
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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.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
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
Protein
: result from protein staining
Intellectual_dis
: individual has intellectual disability (intellectual disability (mental retardation), HP:0001249,mental retardation); please specify
All options:
yes = intellectual disability (HP:0001249, IQ below 70)
borderline = intellectual disability, borderline (HP:0006889, IQ 70-79)
mild = intellectual disability, mild (HP:0001256, IQ 50-69)
moderate = intellectual disability, moderate (HP:0002342, IQ 35-49)
profound = intellectual disability, profound (HP:0002187, IQ below 20)
severe = intellectual disability, severe (HP:0010864, IQ 20-34)
progressive = intellectual disability, progressive (HP:0006887)
no = no intellectual disability (IQ above 79, -)
? = unknown
n/a = not analysed
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158 entries on 2 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Intellectual_dis
Owner
Individual ID
0000026003
Dravet syndrome
-
-
Familial, X-linked dominant, male sparing
-
-
11m
-
-
-
Christel Depienne
00032570
0000026004
epilepsy and mental retardation, female restricted (EFMR)
-
-
Isolated (sporadic)
-
-
-
-
-
-
Christel Depienne
00032571
0000026005
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032572
0000026009
epilepsy, focal; MR
-
-
Isolated (sporadic)
-
-
4y6m
-
-
yes
Johan den Dunnen
00032576
0000026011
Dravet syndrome
-
-
Isolated (sporadic)
-
-
9y
-
-
-
Christel Depienne
00032578
0000026012
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032579
0000026014
epilepsy and mental retardation, female restricted (EFMR)
-
-
Isolated (sporadic)
-
-
14y
-
-
-
Johan den Dunnen
00032581
0000026015
epilepsy, focal; MR
-
-
Isolated (sporadic)
-
-
7y
-
-
yes
Johan den Dunnen
00032582
0000026016
epilepsy, focal; MR
-
-
Isolated (sporadic)
-
-
19y
-
-
yes
Johan den Dunnen
00032583
0000026017
epilepsy and mental retardation, female restricted (EFMR); patIV.2 multiple seizures first year of lif, severe learning disabilities, no speech, behavioral disturbances
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032584
0000026019
Dravet syndrome
-
-
Isolated (sporadic)
-
-
10y
-
-
-
Christel Depienne
00032586
0000026020
Dravet syndrome
-
-
Isolated (sporadic)
-
-
9m
-
-
-
Christel Depienne
00032587
0000026021
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
8y
-
-
-
Christel Depienne
00032588
0000026022
epilepsy, focal
-
-
Isolated (sporadic)
-
-
-
-
-
-
Christel Depienne
00032589
0000026024
epilepsy and mental retardation, female restricted (EFMR)
-
-
Isolated (sporadic)
-
-
6y
-
-
-
Johan den Dunnen
00032591
0000026027
epilepsy, focal; MR
-
-
Isolated (sporadic)
-
-
11y
-
-
yes
Johan den Dunnen
00032594
0000026028
epilepsy, focal; MR
-
-
Isolated (sporadic)
-
-
6y
-
-
yes
Johan den Dunnen
00032595
0000026029
Dravet syndrome
-
-
Isolated (sporadic)
-
-
7y
-
-
-
Johan den Dunnen
00032596
0000026030
Dravet syndrome
-
-
Isolated (sporadic)
-
-
10y
-
-
-
Johan den Dunnen
00032597
0000026031
Dravet syndrome; epilepsy, generalized; seizures, focal and secondary generalization; EFMR
-
-
Isolated (sporadic)
-
-
-
-
-
-
Johan den Dunnen
00032598
0000026033
Dravet syndrome
-
-
Isolated (sporadic)
-
-
6y
-
-
-
Johan den Dunnen
00032600
0000026034
epilepsy and mental retardation, female restricted (EFMR)
-
-
Isolated (sporadic)
-
-
13y
-
-
-
Johan den Dunnen
00032601
0000026035
Dravet syndrome
-
-
Isolated (sporadic)
-
-
8m
-
-
-
Christel Depienne
00032602
0000026036
Dravet syndrome
-
-
Isolated (sporadic)
-
-
9m
-
-
-
Christel Depienne
00032603
0000026037
epilepsy, generalized; MR
-
-
Isolated (sporadic)
-
-
8y
-
-
yes
Johan den Dunnen
00032604
0000026040
Dravet syndrome
-
-
Isolated (sporadic)
-
-
-
-
-
-
Christel Depienne
00032607
0000026042
Dravet syndrome
-
-
Isolated (sporadic)
-
-
-
-
-
-
Christel Depienne
00032609
0000026043
Dravet syndrome
-
-
Isolated (sporadic)
-
-
8y
-
-
-
Johan den Dunnen
00032610
0000026044
Dravet syndrome
-
-
Isolated (sporadic)
-
-
7y
-
-
-
Johan den Dunnen
00032611
0000026045
Dravet syndrome
-
-
Isolated (sporadic)
-
-
9y
-
-
-
Johan den Dunnen
00032612
0000026047
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032614
0000026049
Dravet syndrome
-
-
Isolated (sporadic)
-
-
8m
-
-
-
Christel Depienne
00032616
0000026050
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032617
0000026051
Dravet syndrome
-
-
Unknown
-
-
11y
-
-
-
Christel Depienne
00032618
0000026052
Dravet syndrome
-
-
Unknown
-
-
-
-
-
-
Christel Depienne
00032619
0000026053
Dravet syndrome
-
-
Isolated (sporadic)
-
-
15y
-
-
-
Christel Depienne
00032620
0000026054
Dravet syndrome
-
-
Isolated (sporadic)
-
-
8y
-
-
-
Christel Depienne
00032621
0000026057
Dravet syndrome
-
-
Isolated (sporadic)
-
-
11y
-
-
-
Christel Depienne
00032624
0000026058
Dravet syndrome, adolescence-onset idiopathic epilepsy
-
-
Unknown
-
-
9m
-
-
-
Christel Depienne
00032625
0000026059
epilepsy, focal, no mental retardation
-
-
Familial
-
-
7y
-
-
no
Christel Depienne
00032626
0000026063
Dravet syndrome
-
-
Isolated (sporadic)
-
-
-
-
-
-
Christel Depienne
00032630
0000026064
Dravet syndrome
-
-
Isolated (sporadic)
-
-
60y
-
-
-
Christel Depienne
00032631
0000026068
Dravet syndrome
-
-
Isolated (sporadic)
-
-
8y
-
-
-
Christel Depienne
00032635
0000026069
epilepsy and mental retardation, female restricted (EFMR)
-
-
Isolated (sporadic)
-
-
8y
-
-
-
Johan den Dunnen
00032636
0000026071
epilepsy and mental retardation, female restricted (EFMR)
-
-
Isolated (sporadic)
-
-
18y
-
-
-
Johan den Dunnen
00032638
0000026072
epilepsy, focal; MR
-
-
Isolated (sporadic)
-
-
8y
-
-
yes
Johan den Dunnen
00032639
0000026073
Dravet syndrome
-
-
Isolated (sporadic)
-
-
8y
-
-
-
Johan den Dunnen
00032640
0000026074
Dravet syndrome
-
-
Unknown
-
-
9m
-
-
-
Christel Depienne
00032641
0000026076
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032643
0000026077
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032644
0000026081
Dravet syndrome
-
-
Isolated (sporadic)
-
-
11m
-
-
-
Christel Depienne
00032648
0000026082
Dravet syndrome
-
-
Isolated (sporadic)
-
-
13y
-
-
-
Christel Depienne
00032649
0000026083
epilepsy and mental retardation, female restricted (EFMR)
-
-
Familial, X-linked dominant, male sparing
-
-
8y
-
-
-
Christel Depienne
00032650
0000026084
epilepsy and mental retardation, female restricted (EFMR)
-
-
Isolated (sporadic)
-
-
9y
-
-
-
Johan den Dunnen
00032651
0000026086
Dravet syndrome; 3/4 females adolescence-onset idiopathic epilepsy
-
-
Familial, X-linked dominant, male sparing
-
-
10m
-
-
-
Christel Depienne
00032653
0000026087
Dravet syndrome
-
-
Isolated (sporadic)
-
-
7m15d
-
-
-
Christel Depienne
00032654
0000026088
Dravet syndrome
-
-
Isolated (sporadic)
-
-
7m15d
-
-
-
Christel Depienne
00032655
0000026090
Dravet syndrome; epilepsy, focal
-
-
Isolated (sporadic)
-
-
14y
-
-
-
Christel Depienne
00032657
0000026092
Dravet syndrome
-
-
Isolated (sporadic)
-
-
12m
-
-
-
Christel Depienne
00032659
0000026093
Dravet syndrome
-
-
Isolated (sporadic)
-
-
8y
-
-
-
Christel Depienne
00032660
0000026094
Dravet syndrome; epilepsy, focal
-
-
Isolated (sporadic)
-
-
15y
-
-
-
Christel Depienne
00032661
0000026125
epilepsy; autism spectrum disorder; sisters resp. infantile seizures/Aspergerís syndrome and epilepsy/mild intellectual disability
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Johan den Dunnen
00032692
0000026133
see paper: ..
-
-
Unknown
-
-
-
-
-
-
Christel Depienne
00032700
0000026134
see paper: ..
-
-
Unknown
-
-
-
-
-
-
Christel Depienne
00032701
0000026136
see paper: ..
-
-
Unknown
-
-
7m15d
-
-
-
Christel Depienne
00032703
0000026140
see paper: ..
-
-
Unknown
-
-
-
-
-
-
Christel Depienne
00032707
0000026141
see paper: ..
-
-
Familial, X-linked dominant, male sparing
-
-
-
-
-
-
Christel Depienne
00032708
0000029035
tonic-clonic seizures, anterior slow spikes and waves on the EEG, vermis atrophia, central myelination delay, severe psychomotor delay and intellectual disability, cerebellar syndrome, behavioral troubles
-
-
Isolated (sporadic)
-
-
06y
-
-
yes
Sophie Nambot
00038516
0000029037
Flexion and clonic spasms of the upper limbs with eye rolling, loss of consciousness and hypotonia in the post-critical phase. show. Disorganized vigil and sleep pattern with suspect bitemporal pattern on the EEG .
-
-
Isolated (sporadic)
-
-
00y02m
-
-
severe
Sophie Nambot
00038515
0000029038
West syndrome with infantile spams and hypsarrhythmia, poly spikes and disorganized pattern on the EEG, cortico-cortical atrophy on the MRI
-
-
Isolated (sporadic)
-
-
00y06m
-
-
severe
Sophie Nambot
00038520
0000029041
absences, Diffuses spikes waves, slow wakefulness pattern, White matter, posterior U fibers and splenium lesions, myelinisation delay of the anterior arms of the intern capsules.
-
-
Isolated (sporadic)
-
-
05y
-
-
severe
Sophie Nambot
00038521
0000041531
ataxia, ID, spasticity, epilepsy
cerebellar ataxia
EIEE13
Isolated (sporadic)
-
-
00y06m
-
-
-
Erik-Jan Kamsteeg
00054867
0000054276
18y old male with seizures tarting from 8m of age and mild ID.
-
-
Isolated (sporadic)
18y
18y
00y08m
-
-
mild
Bernt Popp
00074453
0000054277
8y old female with seizures and encephalopathy with onset at age 4m and severe ID with regression.
-
-
Isolated (sporadic)
08y
08y
00y04m
-
-
severe
Bernt Popp
00074454
0000078638
severe early infantile encephalopathy (global) hyperkinetic stereotypic movements "oculogyric like" eye movements
-
-
Isolated (sporadic)
02y
-
00y02m
-
-
profound
Ronen Spiegel
00100436
0000083721
regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), generalized tonicclonic seizures (HP:0002069), spasticity (HP:0001257), impaired volitional movement (HP:?)
-
-
Familial, autosomal recessive
-
-
01y06m
-
-
-
Jamie Zeegers
00072245
0000083722
no regression (-HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), ballism (HP:0100248), multifocal (HP:0030651), intractable (HP:?), hypotonia (HP:0001252), impaired volitional movement (HP:?)
-
-
Familial, autosomal recessive
-
-
00y04m
-
-
-
Jamie Zeegers
00072250
0000083723
regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), cogwheel rigidity (HP:0002396), juvenile spasms evolved to LennoxGastaut syndrome (HP:?), hypotonia (HP:0001252), impaired volitional movement (HP:?), horizontal nystagmus (HP:0000666), vertical nystagmus (HP:0010544)
-
-
Familial, autosomal recessive
-
-
02y
-
-
-
Jamie Zeegers
00072251
0000083724
regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), myoclonus (HP:0001336), multifocal (HP:0030651), clonic (HP:?), hypotonia (HP:0001252), impaired volitional movement (HP:?)
-
-
Familial, autosomal recessive
-
-
00y06m
-
-
-
Jamie Zeegers
00072252
0000083725
regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), hemiclonic seizures (HP:0006813), generalized tonicclonic seizures (HP:0002069), spasticity (HP:0001257), impaired volitional movement (HP:?)
-
-
Familial, autosomal recessive
-
-
01y10m
-
-
-
Jamie Zeegers
00072246
0000083726
regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), hemiclonic seizures (HP:0006813), spasticity (HP:0001257), impaired volitional movement (HP:?)
-
-
Familial, autosomal recessive
-
-
01y10m
-
-
-
Jamie Zeegers
00072247
0000083727
regression (HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), later rigidity (HP:0002063), hypokinesia (HP:0002375), hemiclonic seizures (HP:0006813), generalized seizures (HP:0002197), spasticity (HP:0001257), impaired volitional movement (HP:?)
-
-
Familial, autosomal recessive
-
-
01y10m
-
-
-
Jamie Zeegers
00072248
0000083728
no regression (-HP:0002376), intellectual impairment (HP:0100543), no expressive speech (HP:0000750), chorea (HP:0002072), hemiclonic seizures (HP:0006813), no neuromotor impairment (-HP:?)
-
-
Familial, autosomal recessive
-
-
02y
-
-
-
Jamie Zeegers
00072249
0000141809
-
-
-
Familial, autosomal recessive
-
-
-
-
-
-
Anaïs Begemann
00176985
0000141812
-
-
-
Familial, autosomal dominant
-
-
-
-
-
-
Anaïs Begemann
00176996
0000141814
HP:0000160 HP:0001252 HP:0002078 HP:0002313 HP:0000565
-
-
Familial, autosomal recessive
-
-
-
HP:0003623
-
-
Anaïs Begemann
00176997
0000143155
-
-
-
Familial, autosomal dominant
-
-
00y01m
-
-
profound
Anaïs Begemann
00180892
0000143156
-
-
-
Familial, autosomal dominant
-
-
-
-
-
profound
Anaïs Begemann
00180891
0000155293
Epilepsy, focal seizures with hypertonicity which evolved during childhood to include atypical absence seizures, tonic seizures and atonic (drop) attacks. Choreoathetoid movements. Blepharitis. Vision and hearing are normal but speech is absent. Global DD. No congenital malformations such as cleft palate or congenital heart disease.
-
-
Familial, X-linked
-
-
00y04m
-
-
-
Philippe Campeau
00207516
0000155294
Seizures
-
-
Familial, X-linked
-
-
-
-
-
-
Philippe Campeau
00207517
0000155295
High anterior hairline, upslanted palpebral fissures, a depressed nasal bridge, short nose with anteverted nares, malar flattening, a long philtrum, a thin vermilion of the lips, down‐turned corners of the mouth, micrognathia, a cleft soft palate, large and uplifted earlobes, an overfolded helix of the left ear, and a short neck. Widely spaced nipples. Severe muscular hypotonia and multiple contractures involving the elbows, wrists, fingers, hips and knees, short limbs, and rocker‐bottom feet. Small cerebellum, white‐matter immaturity, prominent sulci, and small optic nerves. Tonic seizures with ocular deviation. Hepatosplenomegaly and developed sepsis from necrotizing enterocolitis. Echochardiography showed a persistent foramen ovale and mild pulmonary hypertension. ALP level not recorded.
-
EIEE
Familial, X-linked
-
-
-
-
-
-
Philippe Campeau
00207518
0000172719
-
epileptic encephalopathy
EIEE-26
Isolated (sporadic)
-
-
-
-
-
-
Giulia Barcia
00228773
0000172993
does not walk; speaks few short words; comprehension severely limited; no regression; severe DD or ID; 2m-onset seizures; no MRI anomalies; truncal hypotonia; hypertonia lower limbs; paroxysmal movement disorder; no stereotypies; limited interaction, easy smiling and laughing; face Pitt-Hopkins-like; 6-7m-transient strabismus, mild constipation
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
8y4m
-
-
-
-
-
Johan den Dunnen
00229787
0000172994
2.5y-does not walk ; no speech; comprehension limited; no regression; severe DD or ID; 4d-onset seizures (generalized); delayed myelinationMRI ; hypotonia; choreatic, dystonic, paroxysmal dyskinetic attacks; no stereotypies; no behavioral anomalies ; low nasal bridge, epicanthal folds
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
3y6m
-
-
-
-
-
Johan den Dunnen
00229788
0000172995
does not walk; no speech; comprehension turns to voice only; 6m-regression; profound DD or ID; 6m-onset seizures (status epilepticus); MRI enlarged ventricles, prominent cortical sulci, thin corpus callosum; hypotonia; dystonic movement disorder; no stereotypies; no behavioral anomalies; hirsute long eyelashes, micrognathia, large pinnae; 3y-left hemiplegia after status epilepticus
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
8y
-
-
-
-
-
Johan den Dunnen
00229789
0000172996
does not walk; no speech; comprehension limited; regression after seizures; severe DD or ID; 10w-onset seizures (focal, sec. generalized; later status epilepticus); MRI thin corpus callosum, cerebellar hypoplasia, prominent opercula, later cortical atrophy; truncal hypotonia; hypertonia limbs; no movement disorder; stereotypic hand movements; no behavioral anomalies ; sparse eyebrows, deep-set eyes, depressed nasal root, slightly low insertion of columella; hemiparesis after status epilepticus
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
11y
-
-
-
-
-
Johan den Dunnen
00229790
0000172997
walks with support; no speech; no comprehension ; regression; severe DD or ID (IQ <30); 4w-onset seizures (2x status epilepticus); MRI secondarily acute diffusion and white-matter abnormalities, atrophy; hypotonia; movement disorder; no stereotypies; pleasant behavior; full lower lip, flat maxillae; 14y-acute onset of hemiparesis during febrile short-lasting seizure
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
14y
-
-
-
-
-
Johan den Dunnen
00229791
0000172998
walks short distances; no speech; comprehension severely limited; 4m-possible regression; severe DD or ID; 4m-onset seizures; no MRI anomalies; hypotonia; no hypertonia; dystonic movement disorder; stereotypic repetitive behaviors; noise sensitivity, self-harm (exacerbated by anxiety); deep-set eyes, epicanthal folds, low anterior hairline, thick arched eyebrows, broad nasal tip
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
17y
-
-
-
-
-
Johan den Dunnen
00229792
0000172999
5y-walks few steps; no speech; comprehension severely limited; no regression; severe DD or ID; 4m-onset seizures (complex partial, generalized tonic clonic); no MRI anomalies; truncal hypotonia; hypertonia limbs; paroxysmal, dystonic-athetoid attacks; no stereotypies; behavioral anomalies; dolichocephaly, wide-spaced teeth; hyperreflexia, mild oculomotor apraxia, insomnia, constipation
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
7y
-
-
-
-
-
Johan den Dunnen
00229793
0000173000
3y-walks; speaks few short words; comprehension good; 3y-regression; moderate DD or ID; 3y-onset seizures (focal status); MRI right hemispheric swelling after left hemiplegia and focal seizures; axial hypotonia; hypertonia mild left spastic hemiparesis; paroxysmal dystonic attacks; no stereotypies; no behavioral anomalies ; slightly smooth philtrum; left hemiplegia, bilateral fifth-finger clinodactyly
early infantil epileptic encephalopathy
EIEE-64
Isolated (sporadic)
3y
-
-
-
-
-
Johan den Dunnen
00229794
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