All individuals with variants in gene CYP51A1

5 entries on 1 page. Showing entries 1 - 5.
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00065053 - PubMed: Gillespie 2014, Journal: Gillespie 2014 no family history M no - - - - - - CCTRCT nuclear, lamellar cataract; developmental delay, spastic diplegia, cryptogenic neonatal liver cirrhosis 2 1 Johan den Dunnen
00441888 Cata_DGU-16;Fam23 PubMed: Aldahmesh 2012, PubMed: Khan 2015 family, 1 affected, unaffected heterozygous parents - yes Saudi Arabia - - - - - CTRCT congenital cataract, total white 1 1 Johan den Dunnen
00444941 10DG1249 PubMed: Patel 2017 family - - - - - - - - CTRCT congenital cataract; not syndromic 1 2 Johan den Dunnen
00444984 16DG0226 PubMed: Patel 2017 5-generation family, 5 affected (2F, M, 2 fetuses), unaffected hetarozygous carrier parents/relatives F;M - - - - - - - CTRCT congenital cataract, neonatal fulminant hepatic failure and global developmental delay; syndromic 1 5 Johan den Dunnen
00468469 Pat28 PubMed: Wang 2024 patient, no family history F - China - - - - - CTRCT zonular cataract, pulverulent cataract; symmetrical opacities; liver disease 2 1 Johan den Dunnen
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