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患有特纳综合征的水肿胎儿合并脑积水：一种罕见的关联。

Hydrocephalus in a hydropic fetus with Turner syndrome: a rare association.

作者信息

Kalpatthi R, Lieber E, Rajegowda B, Sharma J

机构信息

Division of Pediatric Cardiology, Lincoln Medical and Mental Health Center, Bronx, New York, USA.

出版信息

J Matern Fetal Neonatal Med. 2003 Aug;14(2):136-8. doi: 10.1080/jmf.14.2.136.138.

DOI:10.1080/jmf.14.2.136.138
PMID:14629097
Abstract

We report a rare case of antenatally diagnosed Turner syndrome associated with hydrocephalus. In addition, the fetus had cystic hygroma, hydrops fetalis and hypoplastic left heart syndrome. Pregnancy was terminated because of the poor outcome of the above-mentioned anomalies. A possible mechanism for the development of hydrocephalus is discussed.

摘要

我们报告一例罕见的产前诊断为特纳综合征并伴有脑积水的病例。此外，该胎儿还患有颈部水囊瘤、胎儿水肿和左心发育不全综合征。由于上述异常情况预后不良，妊娠被终止。本文还讨论了脑积水发生的可能机制。

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Hydrocephalus in a hydropic fetus with Turner syndrome: a rare association.患有特纳综合征的水肿胎儿合并脑积水：一种罕见的关联。
J Matern Fetal Neonatal Med. 2003 Aug;14(2):136-8. doi: 10.1080/jmf.14.2.136.138.
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Third trimester resolution of cystic hygroma and pleural effusion in a fetus with Turner syndrome.患有特纳综合征胎儿的囊性水瘤和胸腔积液在孕晚期消退
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Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome.Turner综合征中胎儿囊状水瘤和水肿的自然消退
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Resolution of cystic hygroma, hydrops fetalis, and fetal anemia.囊状水瘤、胎儿水肿和胎儿贫血的消退。
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A case report of Turner syndrome associated with fetal nuchal cystic hygroma and bilateral syndactyly of the hands and feet.特纳综合征合并胎儿颈项透明层囊状水肿及手足并指（趾）畸形 1 例报告
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