The DRM WebWatcher: Williams Syndrome

	The DRM WebWatcher
	Williams Syndrome
	Updated 3/2004
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Williams syndrome (WS) is a rare genetic condition that can cause both cognitive and medical problems. Most young children with Williams syndrome have similar facial features, heart or blood vessel problems, elevated blood calcium levels, low birth-weight / low weight gain, developmental delays, and other characteristic symptoms. Check out these sites for information about Williams syndrome.

Canadian Association for Williams Syndrome: Information about Williams syndrome, Canadian and online resources, and more.

Comprehensive WS Home Page: The home page of the Williams Syndrome Foundation, this extensive site provides a wide range of information about the medical and genetic aspects of WS, behavior and music, family issues, links, and much more.

Moylan Family HomePage: The Moylan family of Ireland, whose daughter has Williams syndrome, offers a good list of links to Williams syndrome organizations, resources, personal home pages, and lists/chats.

Williams-Beuren Syndrome (WBS): A genetic overview from the OMIM (Online Mendelian Information in Man) database.

Williams Syndrome Association (WSA): This nonprofit organization offers information about the syndrome, diagnosis, medical guidelines, educational strategies, links, information about the organization and its services, and more.

Williams Syndrome Monthly Medline Alert: Each month, Karen Scarpelli, the parent of a child with Williams syndrome, posts new medical research and findings on Williams syndrome which appear in the MEDLINE database. The current postings are timely, and the archive of older references dates back to 1995.

Related Subjects: Developmental Disabilities; Rare Disorders; Resources in your state