Alagille syndrome causes
Jump to navigation
Jump to search
Alagille syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Alagille syndrome causes On the Web |
American Roentgen Ray Society Images of Alagille syndrome causes |
Risk calculators and risk factors for Alagille syndrome causes |
Overview
Causes
Alagille syndrome is an autosomal dominant disorder, meaning it can be inherited from one parent who has the disorder. A child who has a parent with Alagille syndrome has a 50 percent chance of developing the disorder. Most people with Alagille syndrome have a mutation, or defect, in the Jagged1 (JAG1) gene. Mutations in the NOTCH2 gene are seen in less than 1 percent of people with Alagille syndrome.