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巴特血红蛋白病继发胎儿水肿。

Hydrops fetalis secondary to Bart hemoglobinopathy.

作者信息

Nakayama R, Yamada D, Steinmiller V, Hsia E, Hale R W

出版信息

Obstet Gynecol. 1986 Feb;67(2):176-80. doi: 10.1097/00006250-198602000-00004.

Abstract

Alpha-thalassemia is the most common cause of hydrops fetalis among Southeast Asians. With the recent influx of Southeast Asian refugees and the rapidly growing Filipino population this will become an increasingly important obstetric problem in the United States. Homozygous alpha-thalassemia, or Bart hemoglobinopathy, is invariably fatal to the fetus and produces significant maternal morbidity. Eighteen cases of homozygous alpha-thalassemia in one hospital are reviewed. This is the largest series reported in the United States. Recommendations are made for antenatal screening, diagnosis, and management of alpha-thalassemia.

摘要

α地中海贫血是东南亚地区胎儿水肿综合征最常见的病因。随着近期东南亚难民的涌入以及菲律宾人口的迅速增长,这在美国将成为一个日益重要的产科问题。纯合子α地中海贫血,即巴氏血红蛋白病,对胎儿总是致命的,并会给母亲带来严重的发病风险。本文回顾了一家医院的18例纯合子α地中海贫血病例。这是美国报告的最大病例系列。文中针对α地中海贫血的产前筛查、诊断及管理提出了建议。

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