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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 41 Issue 9
Sep.  2025
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Guidelines for the diagnosis and treatment of congenital biliary atresia (2025 edition)

DOI: 10.12449/JCH250908
  • Received Date: 2025-07-10
  • Accepted Date: 2025-07-27
  • Published Date: 2025-09-25
  • In order to further standardize the diagnosis and treatment of rare diseases and ensure medical quality and safety, National Health Commission of the People’s Republic of China developed the guidelines for the diagnosis and treatment of 86 diseases in the Second List of Rare Diseases, which were officially released in June 2025, including five rare hepatobiliary diseases of Alagille syndrome, α1-antitrypsin deficiency, congenital biliary atresia, primary biliary cholangitis, and primary sclerosing cholangitis. This article introduces the etiology, epidemiology, clinical manifestations, auxiliary examination, diagnosis, and treatment of Alagille syndrome, in order to provide a reference for clinical practice.

     

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    National Health Commission of the People’s Republic of China. Guidelines for the diagnosis and treatment of 86 rare diseases(2025 edition)[EB/OL].( 2025-06-17)[ 2025-07-10]. https://www.gov.cn/zhengce/zhengceku/202507/content_7031426.htm. https://www.gov.cn/zhengce/-zhengceku/202507/content_7031426.htm

    中华人民共和国国家卫生健康委员会. 86个罕见病病种诊疗指南(2025年版)[EB/OL].( 2025-06-17)[ 2025-07-10]. https://www.gov.cn/zhengce/-zhengceku/202507/content_7031426.htm. https://www.gov.cn/zhengce/-zhengceku/202507/content_7031426.htm
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