Clin Genet. 1991 Feb;39(2):136-41.

Brief clinical report: a 46,XY phenotypic female with Smith-Lemli-Opitz syndrome.

Lachman MF, Wright Y, Whiteman DA, Herson V, Greenstein RM.

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Department of Pathology, Hartford Hospital, CT.

Abstract

A phenotypic female infant with Smith-Lemli-Opitz (SLO) syndrome was found to have a 46,XY karyotype. Autopsy showed normal tests for age and normal Wolffian duct structures. The serum testosterone level was unusually high, suggesting that the failure of virilization of the external genitalia in the child might be due to a defect in testosterone conversion to dihydrotestosterone or a lack of end-organ receptors for the same. An additional feature not previously described in association with SLO syndrome was present, which was clinical hypoglycemia with nesidioblastosis.

PMID:: 1849804; [PubMed - indexed for MEDLINE]

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