Mucopolysaccharidosis

Who to Contact
Where to Go to Chat with Others
Learn More About It
Web Sites
Search Google for "Mucopolysaccharidosis"

Who to Contact

The National MPS Society
PO Box 736
Bangor, ME 04401
207-947-1445
207-990-3074 (fax)
E-mail: info@mpssociety.org
Web: http://www.mpssociety.org/

The National MPS Society's goal is to ultimately find a cure for MPS and ML disorders. The National MPS Society will achieve this goal by supporting research, providing support to individuals and their families affected by an MPS or ML disease, promoting public and professional awareness, and significantly increasing participation by regions.

Where to Go to Chat with Others

• National MPS Society Chat
  For families and friends of people affected by Mucopolysaccharidosis and related diseases. All are welcome

• Morquio
  A group for those affected by Morquio Syndrome
  
  
• Sanfilippo (Mucopolysaccharidosis Yype III)

Learn More About It

• MPS and Mucolipidoses

• Hunter Syndrome information from OMIM

• Hurler Syndrome information from OMIM

• What is Sanfilippo Syndrome?

• Sanfilippo Syndrome A information from OMIM

• Sanfilippo Syndrome B information from OMIM

• Maroteaux-Lamy Syndrome information from OMIM

• Unclassified Types of MPS from OMIM

• Mucopolysaccharidosis Type I H/S - Hurler-Scheie syndrome

• Mucopolysaccharidosis Type IH

• Mucopolysaccharidosis Type II - Hunter Syndrome

• Mucopolysaccharidosis Type III - Sanfilippo syndrome

• Mucopolysaccharidosis Type IS - Scheie syndrome

• Mucopolysaccharidosis Type IV - Morquio syndrome

• Mucopolysaccharidosis Type VI - Maroteaux-Lamy syndrome

• Mucopolysaccharidosis Type VII

Web Sites

• The National MPS Society

• The Canadian MPS Society

• The International Morquio Support Group

• The Ryan Foundation for MPS Children

• Children's Medical Research Foundation - Sanfilippo Syndrome

• MPS I Website

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Last Updated 3/7/07 by familyvillage@waisman.wisc.edu
Document Source: http://www.familyvillage.wisc.edu/lib_muco.htm