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Sanfilippo Syndrome (7)

See Also:
This category in other languages:

French

Sites:

http://www.bensdream.org
» Ben's Dream Open in a new browser window
   Information about a foundation dedicated to increasing awareness of Sanfilippo Syndrome and raising funds to support research aimed at finding a cure. Includes a newsletter.
   http://www.bensdream.org
http://www.claritystudio.com/helpachild/
» Bennett Children's Foundation Open in a new browser window
   Founded by parents of three young children who suffer from Sanfilippo Syndrome, a degenerative genetic disorder that is usually fatal before the teens. Raising awareness of the condition and enlisting financial support.
   http://www.claritystudio.com/helpachild/
http://www.curekirby.org/
» Children's Medical Research Foundation Open in a new browser window
   Funds medical research to find a cure for Sanfilippo Syndrome and other neuro-genetic disorders. News and links to summaries of research that has been supported by the foundation.
   http://www.curekirby.org/
http://www.frankiepants.com
» Frankiepants Open in a new browser window
   Personal site about a child with this disorder. Provides details about the condition.
   http://www.frankiepants.com
http://www.jonahsjustbegun.org
» Jonah's Just Begun Open in a new browser window
   The parents of Jonah Weishaar, who has the rare genetic disease Sanfilippo Syndrome, are setting up the Foundation to Cure Sanfilippo to undertake research into the condition.
   http://www.jonahsjustbegun.org
http://www.mpssociety.org/content/4039/MPS_III/
» MPS III Open in a new browser window
   Information, including the causes, different forms, the inheritance and how the disorder progresses.
   http://www.mpssociety.org/content/4039/MPS_III/
http://www.alifeforelisa.org/
» The Sanfilippo Children's Research Foundation Open in a new browser window
   Canadian based charitable group founded by the parents of Elisa Linton.
   http://www.alifeforelisa.org/

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Last Updated: 2010-07-15 20:59:41



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