Phenotypes for disease #00371 (MCAHS1;GPIBD3 (multiple congenital anomalies, hypotonia, seizures syndrome, type 1 (MCAHS-1, glycosylphosphatidylinositol deficiency, type 3 (GPIBD-3))), OMIM:614080)

7 entries on 1 page. Showing entries 1 - 7.
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0000021049 developmental delay, dysmorphic features, multiple congenital anomalies involving the cardiac, genitourinary and gastrointestinal systems; severe neurological impairment with chorea and seizures leading to early death - - Isolated (sporadic) - - - - - Johan den Dunnen 00016532
0000021051 multiple congenital anomalies including bilateral diaphragmatic hernia, cardiovascular anomalies, segmental renal dysplasia, facial dysmorphism, cleft palate, oligodactyly - - Isolated (sporadic) - - - - - Philippe Campeau 00024935
0000021052 see paper; congenital anomalies, developmental delay, hypotonia, epilepsy, progressive cerebellar atrophy - - Familial, autosomal recessive - - - - - Philippe Campeau 00024936
0000155313 epilepsy, hypotonia, developmental delay, accompanied by nearly normal laboratory test results - - Familial, autosomal recessive - - - - - Philippe Campeau 00207535
0000161610 Severe ID (no social interaction or speech), severe hypotonia, epilepsy/focal seizures. Thin corpus callossum, cerebellar atrophy, increased cerebrospinal fluid spaces, visual impairment (pathological VEP), PEG feeding. Normal serum alkaline phosphatase levels. Appearance: Microcephaly (OFC −4SD), round face, low anterior hairline, broad nasal bridge, high-arched palate, small chin, slender feet and hirsutism. Scoliosis. Dry skin, peeling on feet. - - Familial, autosomal recessive - - - - - Philippe Campeau 00213053
0000161611 Severe ID (no social interaction or speech), severe hypotonia, epilepsy/focal seizures. Thin corpus callossum, PEG feeding. Normal serum alkaline phosphatase levels. Appearance: Bitemporal narrowing, broad nasal bridge, large ears, thin upper-vermillion and a smooth, long philtrum. Scoliosis. Dry skin, peeling on feet. - - Familial, autosomal recessive - - - - - Philippe Campeau 00213134
0000280198 Omphalocele, Hydronephrosis, Echogenic fetal bowel, Increased nuchal translucency, Dextrocardia, Abnormality of ductus venosus blood flow prenatal ultrsound - Familial, autosomal recessive 00y - - - - Andreas Laner 00386391
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