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一种新综合征的产前诊断:全前脑畸形伴运动减退。

Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesia.

作者信息

Morse R P, Rawnsley E, Sargent S K, Graham J M

机构信息

Department of Maternal and Child Health, Dartmouth-Hitchcock Medical Center, Hanover, NH 03756.

出版信息

Prenat Diagn. 1987 Nov;7(9):631-8. doi: 10.1002/pd.1970070905.

Abstract

Markedly decreased fetal activity (akinesia/hypokinesia) is usually readily apparent to experienced mothers, and frequently this concern leads to attempts at prenatal diagnosis. We report prenatal diagnosis of two fetuses with congenital contractures, markedly decreased fetal movement, and microcephaly due to severe holoprosencephaly. Such familial recurrence to phenotypically normal parents suggests a newly recognized autosomal recessive or X-linked syndrome that is readily detectable by prenatal ultrasonography.

摘要

明显减少的胎动(运动不能/运动减退)通常有经验的母亲很容易察觉到,并且这种担忧常常导致进行产前诊断的尝试。我们报告了两例患有先天性挛缩、胎动明显减少且因严重前脑无裂畸形导致小头畸形的胎儿的产前诊断。这种在表型正常的父母中出现的家族性复发提示一种新认识到的常染色体隐性或X连锁综合征,可通过产前超声检查轻易检测到。

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