Synonyms: Alagille-Watson syndrome | Arteriohepatic dysplasia | Syndromic bile duct paucity
A rare syndrome variably characterized by chronic cholestasis due to paucity of intrahepatic bile ducts peripheral pulmonary artery stenosis vertebrae segmentation anomalies characteristic facies posterior embryotoxon/anterior segment abnormalities pigmentary retinopathy and dysplastic kidneys.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version October 2023.
Newly diagnosed with
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Alagille Syndrome Alliance
Cindy Luxhoj Hahn Alaina's Mom President & CEO, Alagille Syndrome Alliance
Global Liver Institute
To improve the lives of individuals and families impacted by liver disease through promoting innovation, encouraging collaboration, and scaling optimal approaches to help eradicate liver diseases.
My Faulty Gene
My Faulty Gene is a nonprofit organization which provides information and assistance to any individual whose family medical history suggests genetic testing might be helpful in identifying an increased risk of disease due to a genetic mutation. We believe that everyone in need of genetic testing should have access to it.
My Little Sunshine Foundation
My Little Sunshine is a non-profit foundation dedicated to educating people about the importance of fertility preservation and making fertility resources accessible to all.
Educate and provide resources to POC with Rare Cancers
Help Hope Live
Help Hope Live assists individuals living with catastrophic injuries and illnesses to fundraise toward their medical expenses and related costs.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
For a list of clinical trials in this disease area, please click here.