National MPS Society, Inc.

Organization URL(s)

info@mpssociety.org
www.mpssociety.org  

Other Contact Information

P.O. Box 736
Bangor, ME 04402-0736

207-947-1445 (Voice)
207-990-3074 (FAX)

Description

The National MPS Society exists to find cures for MPS and related diseases. We provide hope and support for affected individuals and their families through research, advocacy and awareness of these devastating diseases.

Online Resources

• Mucopolysaccharidoses (MPS) I - Hurler, Scheie, and Hurler-Scheie Syndrome
  http://www.mpssociety.org/content/4021/MPS_I/ 
  
• Mucopolysaccharidoses (MPS) II - Hunter Syndrome
  http://www.mpssociety.org/content/4022/MPS_II/ 
  
• Mucopolysaccharidoses (MPS) III - Sanfilippo Syndrome
  http://www.mpssociety.org/content/4039/MPS_III/ 
  
• Mucopolysaccharidoses (MPS) IV - Morquio Syndrome
  http://www.mpssociety.org/content/4040/MPS_IV/ 
  
• Mucopolysaccharidoses (MPS) VI - Maroteaux-Lamy Syndrome
  http://www.mpssociety.org/content/4041/MPS_VI/ 
  
• The National MSP ( mucopolysaccharide ) Society Inc.
  http://www.mpssociety.org/content/4002/MPS__Related_Disorders/ 
  

Print Resources

The MPS Society publishes a quarterly magazine for its members. We also offer Syndrome booklets as well a management, Education, Anesthesia and Daily Living Guide. For more information, please contact the society.

Related Topics

Demyelinating Diseases Diagnostic Test Endocrine Diseases Genetics Mental Retardation Mucolipidosis

Review Date

Sat Mar 11, 2006