Phenotypes for disease #05365 (NEDHCAS (neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures), OMIM:618879)

23 entries on 1 page. Showing entries 1 - 23.
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0000119740 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147023
0000119741 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147024
0000119742 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147025
0000119743 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147026
0000119744 - - see paper; ... Familial, autosomal recessive - - - - Johan den Dunnen 00147027
0000155300 - - Global developmental delay; muscular hypotonia; febrile seizures; decreased activity of mitochondrial complex II Familial, autosomal recessive - - - - Philippe Campeau 00207523
0000155304 - - Ichthyosiform dermatosis at birth. Dysmorphic facial features (hypertelorism, brachycephaly, epicanthal folds, flat broad nasal root, full lips, widely spaced teeth, overfolded helices, thickened palms and soles. Myoclonic jerks evoked by sudden unexpected acoustic or tactile stimuli. Focal seizures. DD. Severe ID. Ear anomalies. Transient apnea. Normal serum ALP. No retinal coloboma, congenital heart defects or hearing loss. No renal abnormalities. Normal brain MRI. Familial, autosomal recessive 02y - - - Philippe Campeau 00207526
0000155305 - - Ichthyosiform dermatosis at birth. Dysmorphic facial features (hypertelorism, brachycephaly, epicanthal folds, flat broad nasal root, full lips, widely spaced teeth, overfolded helices, thickened palms and soles. DD. Severe ID. Ear anomalies. Myoclonic and focal seizures. Transient apnea. Normal serum ALP. No retinal coloboma, congenital heart defects or hearing loss. No renal abnormalities. Normal brain MRI. Unknown 09y - - - Philippe Campeau 00207527
0000155306 - - During pregnancy: foetal ultrasound shows congenital hydronephrosis. Ichthyosiform dermatosis at birth. Dysmorphic facial features (hypertelorism, brachycephaly, epicanthal folds, flat broad nasal root, full lips, widely spaced teeth, overfolded helices, thickened palms and soles. DD. Severe ID. Ear anomalies. Seizures: myoclonic, focal, absence, atonic. Transient apnea. Normal serum ALP. No retinal coloboma, congenital heart defects or hearing loss. Unknown 13y - 2d - Philippe Campeau 00207528
0000222963 - - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; movement disorder; epilepsy/seizures; dysmorphisms; ophthalmological anomalies; genito-urinary malformation; no gastrointestinal anomalies; teeth anomalies; hand/foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Philippe Campeau 00289333
0000223735 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; ataxia; epilepsy/seizures; dysmorphisms; no ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; teeth anomalies; hand/foot anomalies; skeletal findings; low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00289334
0000223736 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; ataxia; no epilepsy/no seizures; dysmorphisms; ophthalmological anomalies; no genito-urinary malformation; gastrointestinal anomalies including gastroesophageal reflux disease; no teeth anomalies; no hand/no foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00289335
0000223737 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; ataxia; no epilepsy/no seizures; dysmorphisms; ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; no teeth anomalies; no hand/no foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00289336
0000223738 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; ataxia; no epilepsy/no seizures; no dysmorphisms; no ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; no teeth anomalies; no hand/no foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00289337
0000223739 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; movement disorder; epilepsy/seizures; dysmorphisms; no ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; teeth anomalies; no hand/no foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00289338
0000223740 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; -; ataxia; epilepsy/seizures; no dysmorphisms; ophthalmological anomalies; no genito-urinary malformation; gastrointestinal anomalies including gastroesophageal reflux disease; no teeth anomalies; no hand/no foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00289339
0000223741 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; no movement disorder; epilepsy/seizures; no dysmorphisms; ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; no teeth anomalies; no hand/no foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00289340
0000223742 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; no movement disorder; epilepsy/seizures; dysmorphisms; ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; teeth anomalies; no hand/no foot anomalies; no skeletal findings Familial, autosomal recessive - - - - Johan den Dunnen 00289341
0000223743 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; -; movement disorder; no epilepsy/no seizures; dysmorphisms; no ophthalmological anomalies; genito-urinary malformation; no gastrointestinal anomalies; no teeth anomalies; no hand/no foot anomalies; no skeletal findings; no low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00296268
0000223744 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; ataxia; epilepsy/seizures; dysmorphisms; ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; teeth anomalies; hand/foot anomalies; skeletal findings; low serum alkaline phosphatase Familial, autosomal recessive - - - - Johan den Dunnen 00296269
0000223745 glycosylphosphatidylinositol biosynthesis defect - hypotonia; developmental disability and/or intellectual disability; cerebellar atrophy; no movement disorder; epilepsy/seizures; dysmorphisms; ophthalmological anomalies; no genito-urinary malformation; no gastrointestinal anomalies; no teeth anomalies; no hand/no foot anomalies; no skeletal findings Familial, autosomal recessive - - - - Johan den Dunnen 00296270
0000235902 glycosylphosphatidylinositol biosynthesis defect GPIBD17 - Familial, autosomal recessive - - - - Johan den Dunnen 00309913
0000341357 - NEDHCAS Triggered by infection, Episodic ataxia, Intellectual disability, Delayed fine motor development; parents consanguineous (cousin and cousin), son of the father's cousin with similar symptoms (also ataxia esp. in the context of infections) Familial, autosomal recessive 01y - - - Andreas Laner 00452750
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