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作 者:曾石江 戚子惠[1,2,3] 刘庆春[1,2,3]
机构地区:[1]茂名市人民医院超声室 [2]茂名市人民医院检验科 [3]茂名市人民医院妇产科
出 处:《中国医学影像学杂志》1996年第1期35-37,共3页Chinese Journal of Medical Imaging
摘 要:α-地中海性贫血Ⅰ的纯合子,称HbBart's胎儿水肿综合征,较为少见。1988.05~1994.12临床超声检查发现HbBart's胎儿水肿综合征38例,说明本病在粤西地区并非少见。罹病胎儿均有腹水,部份病例并有胸水;肝、脾肿大;以及巨大、苍白和易碎裂的胎盘。The alpha-thalassemia is a rare disease Their homozygotes (a-thal 1/a-thal 1) are called Hb Bart's hydrops fetalis syndrome Thirty-eight cases had been diagnosed with ultrasonography from May 1988 to December 1994, showing that this syndrome was not uncommon in the west of Guangdong Province All of the fetal patients had ascites and a portion of them had hydrothorax and hepatosplenomegaly Their placentae were large, thick, pale and friable All the cases were verified by induced labour and some of them were identified by the hemoglobin electrophoresis with cord blood or the polymerase chain reaction with blood of their parents
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