- Alagille-Watson syndrome
- Arteriohepatic dysplasia
- Cardiovertebral syndrome
- Cholestasis with peripheral pulmonary stenosis
- Hepatic ductular hypoplasia
- GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions. Click on the link to view the article on this topic.
The Childhood Liver Disease Research and Education Network (ChiLDREN) is a team of doctors, nurses, research coordinators, and research labs throughout the U.S., working together to improve the lives of people with rare liver diseases through research. Current studies are enrolling people with Alagille syndrome, alpha one-antitrypsin deficiency, bile acid synthesis defects, biliary atresia, cystic fibrosis liver disease, idiopathic neonatal hepatitis, mitochondrial hepatopathies, and progressive familial intrahepatic cholestasis. Click on the link above to learn more.
Visit the following link to find the participating research center nearest you.
- ClinicalTrials.gov lists trials that are studying or have studied Alagille syndrome. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.