All individuals with variants in gene PCDHGA3

6 entries on 1 page. Showing entries 1 - 6.
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00050182 - PubMed: DDDS 2015, Journal: DDDS 2015 proband - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00050575 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, seizures 1 1 Johan den Dunnen
00056044 - PubMed: Riviere 2012, Journal: Riviere 2012, PubMed: Mirzaa 2012 - M - - - >00y11m - - - ? MCAP/MMPH overlap patient; MCAP-like features, congenital megalencephaly (HP:0001355, 7.5m OFC +5.5), somatic asymmetry, vascular malformations, connective tissue dysplasia (skin laxity, joint hypermobility, thick doughy subcutaneous tissue), poorly-substantiated umbilical hemangioma; MRI-brain megalencephaly, mild ventriculomegaly (HP:0002119), polymicrogyria (HP:0002126), cerebellar tonsillar ectopia; hydrocephalus (HP:0000238), no skin capillary malformations, no distal limb anomalies (no polydactyly (-HP:0010442), no syndactyly (-HP:0001159)) 1 1 Johan den Dunnen
00226142 FamPatIII1 PubMed: Shukla 2019, Journal: Shukla 2019 3-generation family, unaffected heterozygous carrier parents M - India - - - - - RPIAD see paper; ..., developmental delay; speech delay; epilepsy; regression; dysarthria; no nystagmus; ataxia; spasticity; exaggerated deep tendon reflexes; extensor plantar reflex; increased urine polyol levels; retinitis pigmentosa; cerebral white matter abnormalities; no hearing loss; EEG slow right frontal discharge with epileptiform activity 2 1 Anju Shukla
00231412 Fam4527 PubMed: Cox 2019 4-generation family, 6 affected (3F, 3M) F;M - United States - - - - - CLP vertebral hyper segmentation (HP:0003422), rib hyper segmentation (HP:0006655) 1 6 Timothy Cox
00265203 Pat PubMed: Kiselev 2019 - F - Sweden - - - - - MD see paper; ..., cardiomyopathy, limb-girdle type muscular dystrophy 1 1 Johan den Dunnen
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