Δ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomes-Reference-Cited by-同舟云学术

Δ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomes

Published:2019-02-21 Issue:7 Volume:25 Page:859-869
ISSN:1007-9327
Container-title:World Journal of Gastroenterology
language:
Short-container-title:WJG

Author:

Zhang Mei-Hong,Setchell Kenneth DR,Zhao Jing,Gong Jing-Yu,Lu Yi,Wang Jian-She

Publisher

Baishideng Publishing Group Inc.

Subject

Gastroenterology,General Medicine

Reference35 articles.

1. Disorders of bile acid synthesis and metabolism

2. Defects in Bile Acid Biosynthesis-Diagnosis and Treatment

3. Delta 4-3-oxosteroid 5 beta-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis.

4. Setchell KDR, Flick R, Watkins JB, Piccoli DA. Chronic hepatitis in a 10 yr old due to an inborn error in bile acid synthesis—diagnosis and treatment with oral bile acid. Gastroenterology 1990; 98: A578

5. Cholestatic liver disease in adults may be due to an inherited defect in bile acid biosynthesis

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