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动脉肝发育不良:表型特征与家系研究。

Arteriohepatic dysplasia: phenotypic features and family studies.

作者信息

Mueller R F, Pagon R A, Pepin M G, Haas J E, Kawabori I, Stevenson J G, Stephan M J, Blumhagen J D, Christie D L

出版信息

Clin Genet. 1984 Apr;25(4):323-31. doi: 10.1111/j.1399-0004.1984.tb01998.x.

Abstract

Arteriohepatic dysplasia (AHD) is a disorder characterized by intrahepatic cholestasis and peripheral pulmonary artery stenosis. We have reviewed the phenotypic features in the 56 previously reported cases and 7 persons from our institutions with AHD to summarize the type of cardiac, hepatic, facial, ocular and skeletal manifestations observed in this disorder. Family studies evaluating first-degree relatives of patients with AHD are compatible with an autosomal dominant mode of inheritance with reduced penetrance and variable expressivity.

摘要

动脉肝发育不良(AHD)是一种以肝内胆汁淤积和外周肺动脉狭窄为特征的疾病。我们回顾了之前报道的56例病例以及来自我们机构的7例AHD患者的表型特征,以总结该疾病中心脏、肝脏、面部、眼部和骨骼表现的类型。评估AHD患者一级亲属的家族研究结果符合常染色体显性遗传模式,其外显率降低且表现度可变。

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