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一名患有常染色体显性多囊肾病儿童的先天性肝纤维化。

Congenital hepatic fibrosis in a child with autosomal dominant polycystic kidney disease.

作者信息

Kanaheswari Y, Hamzaini A H, Wong S W

机构信息

Department of Paediatrics, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaacob Latiff, Bandar Tun Razak, Cheras, 56000 Kuala Lumpur, Malaysia.

出版信息

Med J Malaysia. 2008 Aug;63(3):251-3.

Abstract

The association of congenital hepatic fibrosis (CHF) with autosomal recessive polycystic kidney disease (ARPKD) is well known and occurs in approximately 50% of cases. However the association of CHF with autosomal dominant polycystic kidney disease (ADPKD) is less well known and less well documented. We report a child with neonatal onset of hypertension due to ADPKD who later develops portal hypertension due to CHF in childhood. A review of this rare association follows.

摘要

先天性肝纤维化(CHF)与常染色体隐性遗传性多囊肾病(ARPKD)的关联已为人熟知,约50%的病例会出现这种情况。然而,CHF与常染色体显性遗传性多囊肾病(ADPKD)的关联则鲜为人知,相关文献记载也较少。我们报告了一名因ADPKD在新生儿期出现高血压的儿童,该儿童在童年期因CHF后来发展为门静脉高压。以下是对这种罕见关联的综述。

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