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先天性甲状腺功能减退症合并卡罗里病和常染色体隐性多囊肾病:病例报告

Congenital hypothyroidism in association with Caroli's disease and autosomal recessive polycystic kidney disease: patient report.

作者信息

Jeha George S, Tatevian Nina, Heptulla Rubina A

机构信息

Department of Pediatric Endocrinology & Metabolism, Texas Children's Hospital, Houston, TX 77030-2399, USA.

出版信息

J Pediatr Endocrinol Metab. 2005 Mar;18(3):315-8. doi: 10.1515/jpem.2005.18.3.315.

Abstract

Autosomal recessive polycystic kidney disease (ARPKD) is an important renal disease of childhood. Congenital hypothyroidism has been associated with glomerulocystic kidney disease, but to date no association has been made with ARPKD. To our knowledge this is the first reported case of congenital hypothyroidism in an infant with ARPKD.

摘要

常染色体隐性多囊肾病(ARPKD)是一种重要的儿童肾脏疾病。先天性甲状腺功能减退症与肾小球囊性肾病有关,但迄今为止尚未发现与ARPKD有关联。据我们所知,这是首例报道的患有ARPKD的婴儿合并先天性甲状腺功能减退症的病例。

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