Journal article
Smith‐Lemli‐Opitz syndrome: phenotypic extreme with minimal clinical findings
Abstract
Smith-Lemli-Opitz syndrome (SLO) is caused by inherited enzymatic deficiency of 7-dehydrocholesterol-delta7-reductase and resultant cholesterol deficiency. It comprises a characteristic combination of facial features, malformations, and mental retardation. We report on three related patients (two brothers and their first cousin) with mental retardation and minimal physical signs in whom the diagnosis of SLO was delayed for a number of years. …
Authors
Nowaczyk MJM; Whelan DT; Hill RE
Journal
American Journal of Medical Genetics, Vol. 78, No. 5, pp. 419–423
Publisher
Wiley
Publication Date
August 6, 1998
DOI
10.1002/(sici)1096-8628(19980806)78:5<419::aid-ajmg5>3.0.co;2-g
ISSN
0148-7299