Novel mutation in the ?-sterol reductase gene in three Lebanese sibs with Smith-Lemli-Opitz (RSH) syndrome

✍ Scribed by Nezarati, Marjan M. ;Loeffler, Judith ;Yoon, Grace ;MacLaren, Linda ;Fung, Ernest ;Snyder, Floyd ;Utermann, Gerd ;Graham, Gail E.

• Publisher: John Wiley and Sons
• Year: 2002
• Tongue: English
• Weight: 205 KB
• Volume: 110
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/ajmg.10367

✦ Synopsis

Abstract

The Smith‐Lemli‐Opitz syndrome (SLOS), or RSH syndrome, is a well‐characterized multiple congenital anomalies/mental retardation syndrome. The phenotype has been redefined to include mildly affected individuals with minor anomalies and developmental delay, and severe malformations with pre‐ and perinatal mortality. The condition is due to the deficient activity of the enzyme 7‐dehydrocholesterol (7‐DHC) reductase [Shefer et al., 1995: J Clin Invest 96:1779–1785], and the gene has been mapped to chromosome 11q13 [Moebius et al., 1998: Proc Natl Acad Sci USA 95:1899–1902]. We describe here a consanguineous family of Syrian‐Lebanese ancestry with three sibs affected with SLOS: two with a mild variant, while the other had severe disease and died in the first year of life. Mutation analysis demonstrated a novel mutation in the DHCR7 gene, present in homozygous form in the two affected individuals available for testing, and heterozygous in the parents. The wide intrafamilial variation of clinical severity in these three sibs is an important finding in SLOS. © 2002 Wiley‐Liss, Inc.