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- W4327898713 abstract "Abstract Neonatal sclerosing cholangitis (NSC) is associated with progressing biliary fibrosis that often requires liver transplantation in childhood. Several recent studies have identified variants in DCDC2 , encoding doublecortin domain‐containing protein 2 (DCDC2), expressed in primary cilia, that accompany syndromic disease and NSC. We report four patients with hepatobiliary disease associated with two novel homozygous or compound heterozygous variants in DCDC2 . Three patients with protein‐truncating variants in DCDC2 , expressing no DCDC2, presented with the originally described severe hepatic phenotype in infancy. One patient with a novel homozygous DCDC2 missense variant shows a markedly milder phenotype only manifest in childhood and with retained DCDC2 expression. Concomitant nephronophthisis is present in three patients and learning disability in two. This report widens the phenotypic spectrum of DCDC2 ‐associated hepatobiliary disease. Testing for DCDC2 expression and DCDC2 variants should be included in the evaluation of cholangiopathy of unknown aetiology in childhood as well as in infancy." @default.
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- W4327898713 date "2023-03-27" @default.
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- W4327898713 title "Biallelic known and novel <scp><i>DCDC2</i></scp> variants in cholestatic liver disease: Phenotype–genotype observations in four children" @default.
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- W4327898713 doi "https://doi.org/10.1111/liv.15563" @default.
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