All individuals with variants in gene PCDHGA10

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
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 1 1 Anju Shukla
00265203 Pat PubMed: Kiselev 2019 - F - Sweden - - - - - MD see paper; ..., cardiomyopathy, limb-girdle type muscular dystrophy 1 1 Johan den Dunnen
00307925 14DG1188 PubMed: Anazi 2017 family M - - - - - - - ID see paper; ..., intellectual disability; abnormal facial shape; bicuspid aortic valve; cleft upper lip; inguinal hernia; recurrent otitis media; microcephaly; brachycephaly; anteverted ears; bulbous nose; long philtrum; thin upper lip vermilion; downturned corners of mouth; synophrys; pes planus; arachnoid cyst 1 1 Johan den Dunnen
00307926 DD_91704 PubMed: Anazi 2017 family M - - - - - - - ID see paper; ..., global developmental delay, congenital microcephaly, infantile spasms, anteverted ears, thin upper lip vermilion, hyperreflexia 1 1 Johan den Dunnen
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