Suppr超能文献

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验