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22三体综合征:孤立性胎儿生长受限的一个原因。

Trisomy 22: a cause of isolated fetal growth restriction.

作者信息

Morrison J J, Hastings R, Jauniaux E

机构信息

Academic Department of Obstetrics and Gynaecology, University College London Medical School, UK.

出版信息

Ultrasound Obstet Gynecol. 1998 Apr;11(4):295-7. doi: 10.1046/j.1469-0705.1998.11040295.x.

Abstract

The management of severe isolated fetal growth restriction at term involves consideration of the risk of associated aneuploidy. A case is described in which intrauterine growth restriction was detected at 37 weeks' gestation in a structurally normal fetus. The diagnosis of trisomy 22 was made after fetal blood sampling. This diagnosis has not been previously reported in a structurally normal fetus. This case highlights the dilemma that arises in the management of the small, structurally normal fetus in the late third trimester. The reasons for survival to term of some trisomy 22 fetuses are as yet unclear and are discussed.

摘要

足月严重孤立性胎儿生长受限的管理涉及对相关非整倍体风险的考量。本文描述了一例病例,在孕37周时于结构正常的胎儿中检测到宫内生长受限。经胎儿血样采集后诊断为22三体。此前尚未有在结构正常胎儿中出现该诊断的报道。该病例凸显了孕晚期结构正常的小胎儿管理中出现的困境。一些22三体胎儿足月存活的原因尚不清楚,本文对此进行了讨论。

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