Alagille syndrome and liver: an adult case report
Abstract Background Alagille syndrome is a rare autosomal-dominant disorder, representing 10 to 15% of the causes of neonatal cholestasis with no gender predominance. The diagnosis is based on the association of liver, heart, eye, skeleton abnormalities, and characteristic facial appearance. Case pr...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
SpringerOpen
2023-11-01
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Series: | Egyptian Liver Journal |
Subjects: | |
Online Access: | https://doi.org/10.1186/s43066-023-00298-0 |