Successful treatment of an infant with congenital bile acid synthesis disorder type 3 by ursodeoxycholic acid: a case report

BACKGROUND: Congenital bile acid synthesis disorder type 3 caused by oxysterol 7α-hydroxylase deficiency is an extremely rare genetic liver disease. As it may cause rapid progression to end-stage liver disease, a high cautiousness in diagnosis and early treatment are required. Here we describe the f...

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Detalles Bibliográficos
Autores principales: Mo, Weiqian, Wang, Feng, Zhou, Chuanen, Ma, Tinghe, Pan, Zhaojun, Xie, Min, Ren, Haoyan, Xie, Yongwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988363/
https://www.ncbi.nlm.nih.gov/pubmed/35387662
http://dx.doi.org/10.1186/s13256-022-03365-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8988363/
https://www.ncbi.nlm.nih.gov/pubmed/35387662
http://dx.doi.org/10.1186/s13256-022-03365-z

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