An Unusual Cause of Cholestasis in an Infant: Biliary Atresia Type IIB
Biliary atresia (BA) is a progressive destructive cholangiopathy of unknown etiology that presents in early infancy. It has a worldwide frequency of 1:8,000–1:15,000 and is common in Asia than in the west. Based on the level at which the lumen of the extrahepatic duct is obliterated, BA is classifie...
Guardado en:
Autores principales: | Poonam Sherwani, Rishi Bolia, Ashish Kaushik, Sumit Kumar, Sanjeev Kishore, Udit Chauhan |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Thieme Medical and Scientific Publishers Pvt. Ltd.
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/15b1962cab0c443289767c2b452177e1 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Biliary Atresia – emerging diagnostic and therapy opportunities
por: Urban Lendahl, et al.
Publicado: (2021) -
Biliary atresia-specific deciduous pulp stem cells feature biliary deficiency
por: Soichiro Sonoda, et al.
Publicado: (2021) -
Rotavirus Infection and Cytopathogenesis in Human Biliary Organoids Potentially Recapitulate Biliary Atresia Development
por: Sunrui Chen, et al.
Publicado: (2020) -
Liver Transplantation for Biliary Atresia in Adulthood: Single-Centre Surgical Experience
por: Miriam Cortes-Cerisuelo, et al.
Publicado: (2021) -
Identifying Biomarkers to Predict the Prognosis of Biliary Atresia by Weighted Gene Co-Expression Network Analysis
por: Meng Kong, et al.
Publicado: (2021)