| Literature DB >> 11562938 |
M J Nowaczyk1, S A Farrell, W L Sirkin, L Velsher, P A Krakowiak, J S Waye, F D Porter.
Abstract
Smith-Lemli-Opitz syndrome (RHS) (SLOS, OMIM 270400) is an autosomal recessive disorder of cholesterol biosynthesis caused by mutations of the 3beta-hydroxysterol Delta(7)-Delta(8)-reductase gene, DHCR7. We report a fetus with holoprosencephaly and multiple congenital anomalies who was homozygous for the IVS8-1G-->C mutation. Following termination of pregnancy, both the elevated amniotic fluid 7-dehydrocholesterol level and the DHCR7 mutations were demonstrated. Two other newborn infants with IVS8-1G-->C/IVS8-1G-->C genotype are described. This report illustrates a severe phenotypic extreme of SLOS associated with a null genotype, underscores the complex relationship between SLOS and holoprosencephaly, and discusses the possible pathogenetic mechanisms of the development of holoprosencephaly in SLOS.Entities:
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Year: 2001 PMID: 11562938 DOI: 10.1002/1096-8628(20010915)103:1<75::aid-ajmg1502>3.0.co;2-r
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299