The purpose of the Alliance is to serve as the main networking resource and source ofinformation for people with AGS, their families, friends, and health care providers.The Alliance is dedicated to increasing public awareness of AGS and supporting research efforts on behalf of the AGS community.
The information presented on this web site is provided for information purposes only. This information does not constitute medical advice and it should not be relied upon as such. The Alagille Syndrome Alliance does not engage in the practice of medicine. Under no circumstances, does the Alagille SyndromeAlliance recommend particular treatments for specific individuals, and in all cases recommends that you consult your physician before pursuingany course of treatment.
