Alagille Syndrome Health Resources


PALF aims at identifying, characterizing, and developing management strategies for infants, children, and adolescents who present with acute liver failure.

This foundation is devoted to providing support for research and education into the causes, diagnoses, prevention and treatment of all liver disease.

CLDF is a unique national charity dedicated to taking action against the effects of all liver diseases of childhood.

The Alagille Syndrome Alliance is an international support network for people with AGS and their families.

GeneTests is a medical genetics information resource developed for physicians, genetic counselors, other healthcare providers and researchers.

ChiLDRN Supports the discovery of new diagnostics, etiologic and treatment options for children with liver disease, and those who undergo liver transplantation.