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Literature DB >> 9893307

An infant with 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase deficiency presenting with typical neonatal hepatitis syndrome: the first Japanese case.

S Terazawa¹, A Kimura, T Inoue, T Murai, T Kurosawa, A Takao.

Abstract

Entities: Disease Species

Mesh：

Substances：

Year: 1998 PMID： 9893307 DOI： 10.1111/j.1442-200x.1998.tb02007.x

Source DB: PubMed Journal: Acta Paediatr Jpn ISSN： 0374-5600

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2 in total

1. Homozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology.

Authors: Vered Molho-Pessach; Jonathan J Rios; Chao Xing; Kenneth D R Setchell; Jonathan C Cohen; Helen H Hobbs
Journal: Hepatology Date: 2012-02-08 Impact factor: 17.425

2. Prognosis and clinical characteristics of patients with 3β-hydroxy-Δ5-C27-steroid dehydrogenase deficiency diagnosed in childhood: A systematic review of the literature.

Authors: Yuan Zhang; Chun-Feng Yang; Wen-Zhen Wang; Yong-Kang Cheng; Chu-Qiao Sheng; Yu-Mei Li
Journal: Medicine (Baltimore) Date: 2022-02-18 Impact factor: 1.817

2 in total