Healthcare Professionals
The ALGSA is very involved in science and research initiatives including many initiatives developed and led right here at the ALGSA. In 2024, the ALGSA is developing the ALGSA Scientific Research Network, expanding on areas of research interest within the community of patients and stakeholders, as well, we are building on our ALGSA Collaborative Scientific Research Grant program that you will see grow this is year.
Current Treatments For ALGS Patients
Find current FDA approved treatment options for patients with Alagille Syndrome and clinical trials.
Participate in GALA Study
The Global ALagille Alliance (GALA) Study is a global initiative to create an international database of clinical, genetic, and laboratory data in children and young adults with Alagille Syndrome (ALGS). The GALA study is led by Principal investigator, Dr. Binita M Kamath….
Alagille Syndrome Educational Resources for Medical Professionals
The ALGSA Resource Library houses guides and manuals, one-page educational resources and tools, and translated materials.
ALGSA Patient & Family Resources
ALGSA develops patient and family resources about ALGS and aspects of the disease. Click to find manuals, guides, one-page educational tools and translated materials.