Screening for
Smith-Lemli-Opitz Syndrome
Škodová J. 1 , Behúlová D. 1 , Nagyová A. 2 , Bzdúch V. 3 , Ponec J. 1 , Kasanická A. 1
1 Oddelenie klinickej biochémie, Detská fakultná nemocnica, Bratislava, Slovenská republika 2 Ústav preventívnej a klinickej medicíny, Bratislava, Slovenská republika 3 I. detská klinika, Detská fakultná nemocnica, Bratislava, Slovenská republika |
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Summary:
The Smith-Lemli-Opitz syndrome (SLOS) is caused by deficiency of 7-dehydrocholesterol-D 7 -reductase, an
essential enzyme in the biosynthesis of cholesterol. Affected patients have low seru m concentrations of chole-
sterol and elevated cholesterol precursors, 7-dehydrocholesterol (7-DHC), 8-dehydrocholesterol and 19-nor-
5,7,9(10)-cholestatrienol. A simple and rapid ultraviolet spectrophotometric (UVS) m ethod for detection of serum
7-DHC is described. Samples of 15 patients with clinical suspicion of SLOS and samples of 6 patients without
symptoms of SLOS were assessed. Absorption maxima characteristics of 7-DHC (lmax 272, 282, and 292 nm) were
observed in 8 patients’ sera but not in controls. In 8 patients’ sera the diagnosis was confirmed biochemically by
gas chromatographic mass spectrometric (GC/MS) analysis of serum sterols. UVS measurement of 7-DHC
correlated well with GC/MS profiles. The UVS assay is cheap and easy method for rapid detection of SLOS in
general clinical biochemical laboratories.
Key words:
Smith-Lemli-Opitz syndrome, screening, 7-dehydrocholesterol, ultraviolet spectrophotometry,
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