David M, Israel N, Merksamer R, Bar-Nizan N, Borochowitz Z, Bar-el H, Yehudai I, Dar H
Simon Winter Institute of Human Genetics, Bnai Zion Medical Center, Haifa, Israel.
Fetal Diagn Ther. 1995 Mar-Apr;10(2):76-9. doi: 10.1159/000264207.
Twenty-four women out of 7,875 pregnant women who enrolled in a prenatal screening program showed extremely low levels of unconjugated estriol (< 0.15 MOM). In 19 cases, intrauterine fetal death was reported. In 1 case anencephalus was detected. In the remaining 4 cases apparently normal healthy babies (1 female and 3 males) were born following uneventful pregnancies. Physical examination of the 3 boys at 4-6 weeks revealed mild ichthyosis compatible with the X-linked type. Two of them had a positive family history of X-linked ichthyosis. The examination of the girl did not reveal any significant findings. In both cases in which amniocentesis was performed, low levels of steroid sulfatase and arylsulfatase C were found. The prevalence of X-linked ichthyosis in this study is higher than previously reported, i.e. 1:1,300 males. Our results suggest that the prenatal screening program for neural tube defects and for Down's syndrome is useful for the prenatal detection of X-linked ichthyosis as well. These results are in accordance with two recent reports. The implications regarding genetic counseling are discussed.
在参加产前筛查项目的7875名孕妇中,有24名孕妇的未结合雌三醇水平极低(<0.15MOM)。其中19例报告发生了宫内胎儿死亡。1例检测出无脑儿。其余4例在孕期顺利后产下了看似正常健康的婴儿(1名女性和3名男性)。对3名男孩在4 - 6周时进行的体格检查发现有与X连锁型相符的轻度鱼鳞病。其中2名男孩有X连锁鱼鳞病的家族阳性史。对女孩的检查未发现任何显著异常。在进行羊膜穿刺术的两例中,发现类固醇硫酸酯酶和芳基硫酸酯酶C水平较低。本研究中X连锁鱼鳞病的患病率高于先前报道,即1:1300男性。我们的结果表明,神经管缺陷和唐氏综合征的产前筛查项目对于X连锁鱼鳞病的产前检测也很有用。这些结果与最近的两份报告一致。文中讨论了其对遗传咨询的意义。