Top/Health/Conditions and Diseases/Genetic Disorders/Sanfilippo Syndrome
Sanfilippo Syndrome :
Sanfilippo Syndrome (MPS III), an autosomal recessive hereditary disorder, is characterized by severe mental deterioration, mild physical defects and the excretion of heparan sulfate in the urine. There are four types of Sanfilippo Syndrome; types A and B are the most common forms.
7 web sites matced for Sanfilippo Syndrome
Ben's Dream
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.
MPS III: Sanfilippo Syndrome
Information, including the causes, different forms, the inheritance and how the disorder progresses.
Children's Medical Research Foundation
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.
Julia's Hope--The Sanfilippo Syndrome Medical Research Foundation, Inc.
A non-profit organization incorporated under the laws of the State of Nebraska to promote research toward a cure for Sanfilippo Syndrome and related disorders in children. Events, grants, and Julia's story.
Special Child: Disorder Zone Archives - Sanfilippo Syndrome
Describes the disorder for the benefit of parents, lists characteristics of children with the disorder, and tells what to expect.
Bennett Children's Foundation
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.
The Sanfilippo Children's Research Foundation
Canadian based charitable group founded by the parents of Elisa Linton.
 
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