Department of Hepatology, The Maria Grzegorzewska University in Warsaw, 02-353 Warsaw, Poland
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Alagille Disorder in Individuals with Cholestatic Liver Conditions: Clinical Characteristics
Author(s): Alice Swan*
Cholestatic liver conditions encompass a group of disorders characterized by impaired bile flow, leading to a build-up of bile acids and other
substances in the liver. Among these conditions, Alagille Syndrome (ALGS) stands out as a rare genetic disorder that affects various organ
systems, with the liver being a central target. ALGS, also known as Alagille-Watson Syndrome or arteriohepatic dysplasia, was first described by
Dr. Daniel Alagille in 1969. It is an autosomal dominant disorder caused by mutations in the JAG1 or NOTCH2 genes, affecting multiple organs
including the liver, heart, skeleton, and eyes. This paper delves into the clinical characteristics of Alagille Disorder in individuals with cholestatic
liver conditions, shedding light on its presentation, diagnosis, and potential therapeutic strategies... Read More»
DOI:
10.37421/2573-4563.2023.7.231
Hepatology and Pancreatic Science received 34 citations as per Google Scholar report