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Smith‐Lemli‐Opitz syndrome: phenotypic extreme...
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