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Alagille Syndrome: A Novel Mutation in JAG1 Gene.

ABSTRACT: Alagille syndrome is an autosomal dominant multisystem disorder with variable phenotypic penetrance, caused by heterozygous mutations in JAG1 or NOTCH2, encoding for the components of the Notch signaling pathway. In this paper, we described a novel mutation not yet reported in literature. This 3-years old male child was referred to our Clinical Genetics Unit because of delayed psychomotor development, systolic murmur, dysmorphic facial features, and hypertransaminasemia. The novel JAG1 heterozygous c.2026delT variant in exon 16 was found. JAG1 mutations are classified as protein truncating and non-protein truncating, without any genotype-phenotype correlation. The detected mutation determines a stop codon (p.Cys676AlafsTer67) in the gene sequence, encoding a truncated protein. Our report broadens the spectrum of JAG1 gene mutations.

SUBMITTER: Fischetto R

PROVIDER: S-EPMC6529843 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Alagille Syndrome: A Novel Mutation in JAG1 Gene.

Fischetto Rita R Palmieri Viviana V VV Tripaldi Maria E ME Gaeta Alberto A Michelucci Angela A Delvecchio Maurizio M Francavilla Ruggiero R Giordano Paola P

Frontiers in pediatrics 20190515

Alagille syndrome is an autosomal dominant multisystem disorder with variable phenotypic penetrance, caused by heterozygous mutations in JAG1 or NOTCH2, encoding for the components of the Notch signaling pathway. In this paper, we described a novel mutation not yet reported in literature. This 3-years old male child was referred to our Clinical Genetics Unit because of delayed psychomotor development, systolic murmur, dysmorphic facial features, and hypertransaminasemia. The novel ...[more]

PMID: 31157196

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