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J-GLOBAL ID:201902235396508673   Reference number:19A1900575

腎移植前精査中にHNF1B異常を同定した先天性腎尿路異常の1例

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Material:
Volume:Issue:Page: 96-98  Publication year: Jul. 31, 2019 
JST Material Number: F1435A  ISSN: 2187-9907  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Congenital diseases,deformities in general.  ,  Clinical medicine on urogenital system in general 
Reference (10):
  • Vivante A, Kohl S, Hwang DY, et al. Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans. Pediatr Nephrol 2014 ; 29 : 695-704.
  • 「腎・泌尿器系の希少・難治性疾患群に関する診断基準. 診療ガイドラインの確立」研究班. 低形成・異形成腎を中心とした先天性腎尿路異常(CAKUT)の腎機能障害進行抑制のためのガイドライン. 東京:診断と治療社, 2016:26-33.
  • 神田祥一郎,服部元史. 先天性腎尿路生殖器症候群(Congenital Urogenital Syndrome). 発達腎研究会誌 2017;21-5.
  • Clissold RL, Hamilton AJ, Hattersley AT, et al. HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum. Nat Rev Nephrol 2015 ; 11 : 102-12.
  • Verhave JC, Bech AP, Wetzels JF, et al. Hepatocyte Nuclear Factor 1β-Associated Kidney Disease : More than Renal Cysts and Diabetes. J Am Soc Nephrol 2016 ; 27 : 345-53.
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