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首页> 外文期刊>Journal of pediatric endocrinology & metabolism: JPEM >Congenital hypothyroidism in association with Caroli's disease and autosomal recessive polycystic kidney disease: patient report.
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Congenital hypothyroidism in association with Caroli's disease and autosomal recessive polycystic kidney disease: patient report.

机译:先天性甲状腺功能减退症与卡罗利氏病和常染色体隐性隐性多囊肾疾病相关:患者报告。

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摘要

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.
机译:常染色体隐性隐性多囊肾病(ARPKD)是儿童期的重要肾脏疾病。先天性甲状腺功能减退症与肾小球囊性肾脏疾病有关,但迄今为止,尚未与ARPKD相关联。据我们所知,这是第一例ARPKD婴儿先天性甲状腺功能减退的病例。

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