PRENATAL DETECTION OF X-LINKED ICHTHYOSIS BY MATERNAL SERUM SCREENING FOR DOWN-SYNDROME

被引:24
作者
BARTELS, I
CAESAR, J
SANCKEN, U
机构
[1] Institute of Human Genetics, University of Göttingen
关键词
ESTRIOL-MATERNAL BLOOD; PRENATAL DIAGNOSIS; DOWN SYNDROME SCREENING; STEROID SULFATASE DEFICIENCY;
D O I
10.1002/pd.1970140316
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Maternal serum unconjugated oestriol (uE3) was measured in 15 375 pregnancies during 2 years of second-trimester risk assessment for Down syndrome using biochemical markers. Very low levels of uE3 (<0.1 MOM) were detected in 22 serum samples (0.14 per cent). Very low uE3 was associated with an adverse outcome in 13 pregnancies including fetal death and miscarriage (N = 11), anencephaly (N = 1), and Meckel-Gruber syndrome (N = 1). Dry scales on the skin appeared in the first year of life in four boys. From dermatological diagnosis, prenatal uE3 levels, and pedigree analysis, it is concluded that at least 5 in approximately 7500 male births in the study population are affected by steroid sulphatase deficiency, which is the biochemical defect in X-linked ichthyosis. Very low uE3 levels in the second trimester are indicative of this disease in pregnancies with normal ultrasound findings.
引用
收藏
页码:227 / 229
页数:3
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