All individuals with variants in gene PCDHB5

2 entries on 1 page. Showing entries 1 - 2.
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00050575 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, seizures 1 1 Johan den Dunnen
00281802 FamA PubMed: Wagner 2020, Journal: Wagner 2020 3-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M - Germany - - - - - NDD severely delayed motor development; no speech development; profound muscular hypotonia; poor head control; no spasticity; reduced upper limb tendon reflexes, reduced lower limb tendon reflexes; infantile spasms; MRI-brain focal thinning of corpus callosum, gray matter heterotopias; dry skin and hypohidrosis; bilateral cataract; normal heart; normal lungs; feeding difficulties, gastrostomy tube; bilateral vesicoureteric reflux grade II; recurrent fever/frequent viral infections; drop foot; craniofacial features thick eyebrows, deep-set eyes, short nasal bridge with anteverted nares, large mouth with prominent lower lip, protruding tongue; gingival hyperplasia 2 1 Johan den Dunnen
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