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FIRST-TRIMESTER DIAGNOSIS OF SMITH–LEMLI–OPITZ SYNDROME

✍ Scribed by P. SHARP; E. HAAN; J. M. FLETCHER; T. Y. KHONG; W. F. CAREY


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
227 KB
Volume
17
Category
Article
ISSN
0197-3851

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✦ Synopsis


We report here the prenatal diagnosis of Smith-Lemli-Opitz (SLO) syndrome in the first trimester by direct measurement of 7-dehydrocholesterol (7-DHC) in a chorionic villus (CV) biopsy. The proband was diagnosed clinically at birth and the diagnosis was confirmed biochemically by demonstrating elevated 7-DHC in plasma. The family pursued prenatal diagnosis in their fourth, fifth, and sixth pregnancies. The fourth pregnancy spontaneously miscarried at 9 weeks' gestation. Analysis in both direct and cultured curetting tissue (identified as similar to CV tissue) showed an abnormal tissue neutral sterol pattern with an elevated 7-DHC concentration. The fifth pregnancy also miscarried spontaneously at 9 weeks but no tissue of unequivocal fetal origin could be identified to allow biochemical investigation. In the sixth pregnancy, ultrasound examination at the time of CV sampling showed a thickened nuchal fold. Direct analysis of the CV sample revealed elevated levels of 7-DHC consistent with the diagnosis of SLO. The pregnancy was terminated and both fetal tissue and cultured fetal cells showed marked increases in 7-DHC, confirming the prenatal diagnosis. 1997 by John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Smith-Lemli-Opitz syndrome
✍ Meinecke, Peter ;Blunck, Werner ;Rodewald, Alexander ;Opitz, John M. ;Reynolds, 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 332 KB 👁 1 views
Prenatal diagnosis of the RSH/Smith-Leml
✍ Kratz, Lisa E.; Kelley, Richard I. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 34 KB 👁 2 views

The RSH/Smith-Lemli-Opitz syndrome (RSH/SLOS) is a relatively common, autosomal recessive malformation syndrome comprising distinctive facial, limb and genital anomalies, and mental retardation. Most patients with a clinical diagnosis of RSH/SLOS have a defect of cholesterol biosynthesis at the leve