Ontology highlight
ABSTRACT:
SUBMITTER: Movassaghi M
PROVIDER: S-EPMC5603413 | biostudies-literature | 2017 Oct
REPOSITORIES: biostudies-literature
Movassaghi Miyad M Bianconi Simona S Feinn Richard R Wassif Christopher A CA Porter Forbes D FD
American journal of medical genetics. Part A 20170810 10
Smith-Lemli-Opitz syndrome (SLOS) is an autosomal recessive congenital malformation syndrome caused by mutations in the 7-dehydrocholesterol reductase gene. This inborn error of cholesterol synthesis leads to elevated concentrations of 7-dehydrocholesterol (7-DHC). 7-DHC also serves as the precursor for vitamin D synthesis. Limited data is available on vitamin D levels in individuals with SLOS. Due to elevated concentrations of 7-DHC, we hypothesized that vitamin D status would be abnormal and p ...[more]