Sanfilippo Syndrome

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Category Description:

Informational sites, organizations and support groups for San Fillippo syndrome, also know as muncopolyaccharidosis (MPS).

  • Alliance Sanfilippo  - Organization dedicated to promoting, supporting, and funding research that lead to curative treatments for Sanfilippo Syndrome.
  • Ben's Dream  - Site created for a young Sanfilippo Syndrome patient. Presents information about the disease, related news and research, and links to other sites of interest.
  • eMedicine  - Contains a clinical reference pertaining to muncopolyaccharidosis Type V11, written by Dr. Donald Nash.
  • MedlinePlus - Sanfilippo syndrome  - Contains a definition, alternative names, causes symptoms, tests, treatment, and the prognosis of MPS III.
  • Medscape Reference: Genetics of Mucopolysaccharidosis Type III  - Provides an overview of the disease and presents its pathophysiology and epidemiology.
  • Team Sanfilippo Foundation  - Nonprofit medical research foundation founded by a group of parents who seek potential therapies that can be tested clinically in the future. Aims to advance research, education, and the quality of life of children affected by the Sanfilippo syndrome.
  • Wrong Diagnosis  - Introduction to the disease also known as Sanfilippo Syndrome and information about its symptoms, causes, treatment, complications, and prognosis. With statistics, videos, and stories.
 
 
 
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