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To provide a support network for people with Alagille Syndrome, enable families to meet other families, support research efforts on AGS, and to increase awareness and understanding of AGS and its symptoms to the general population.
The Alagille Syndrome Alliance is an international support network for people with AGS and their families. The Alliance has grown to several hundred families with AGS located all over the world, all seeking support, understanding, and to share their experiences with others.
- Julie Kelin
- (503) 639-6217
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