新生儿胆汁淤积症揭示先天性巨细胞病毒感染合并阿拉吉尔综合征

Azzouzi F, Abidi K, Elqadiry R, Nassih H, Bourrahouat A, A. I
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引用次数: 0

摘要

家族遗传性肝病可能会从儿童时期的胆汁淤积性黄疸发展到严重的肝功能障碍。虽然先天性巨细胞病毒(cCMV)感染最初会影响健康宿主的肝脏,但慢性肝炎却很少见。我们接诊了一名自出生起就患有胆汁淤积性黄疸的婴儿,其畸形面容显示患有阿拉吉尔综合征,生物检测显示其患有生理性胆汁淤积症,巨细胞病毒血清学检测呈阳性。患者接受了 3 个月的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neonatal Cholestasis Revealing Congenital Cytomegalovirus Infection Combined with Alagille Syndrome
Liver illnesses that run in families might start childhood with cholestatic jaundice and proceed to severe hepatic dysfunction. Although congenital cytomegalovirus (cCMV) infection can initially affect the liver in otherwise healthy hosts, chronic hepatitis is rare. We present an infant with cholestatic jaudnice evolving since birth and dysmorphic facies revealing alagille syndrome, the biological tests is revealing a biological cholestasis and a CMV serology positive. The patient was treated for 3 months.
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