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生殖损失中的细胞遗传学研究。

Cytogenetic studies in reproductive loss.

作者信息

Schmidt R, Nitowsky H M, Dar H

出版信息

JAMA. 1976 Jul 26;236(4):369-73.

PMID:947051
Abstract

Cytogenetic studies were performed on 57 families with pregnancy wastage (eg, two or more spontaneous abortions or stillbirths). Chromosomal abnormalities were ascertained in 17 couples, through offspring with congenital malformations. Seven families had children with neural tube defects, and five families also had a previous child with Down syndrome. One mother had mosaic Turner syndrome; two additional mothers and one father had balanced chromosome translocations. These findings indicate that chromosome analyses should be performed on every couple with repeated miscarriages or malformed children, and subsequent pregnancies at risk should be monitored by amniocentesis.

摘要

对57个有妊娠丢失情况(如两次或更多次自然流产或死产)的家庭进行了细胞遗传学研究。通过患有先天性畸形的后代,在17对夫妇中确定了染色体异常情况。7个家庭的孩子患有神经管缺陷,5个家庭之前还有一个患有唐氏综合征的孩子。一位母亲患有嵌合型特纳综合征;另外两位母亲和一位父亲有平衡染色体易位。这些发现表明,对于每一对有反复流产或畸形儿童的夫妇都应进行染色体分析,对有风险的后续妊娠应通过羊膜穿刺术进行监测。

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