Jeha George S, Tatevian Nina, Heptulla Rubina A
Department of Pediatric Endocrinology & Metabolism, Texas Children's Hospital, Houston, TX 77030-2399, USA.
J Pediatr Endocrinol Metab. 2005 Mar;18(3):315-8. doi: 10.1515/jpem.2005.18.3.315.
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.
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。
