Mucopolysaccharidoses (MPS) and Mucolipidoses (ML)

Cynthia A. Lockley on
  • The Canadian Mucopolysaccharidoses (MPS) Society
  • The National Mucopolysaccharidoses (MPS) Society Mucopolysaccharidoses (MPS) and mucolipidosis (ML) are genetic lysosomal storage diseases (LSD) caused by the body’s inability to produce specific enzymes. The missing or insufficient enzyme prevents cells from recycling waste, resulting in the storage of materials in cells throughout the body. As the disease progresses, there is widespread damage throughout the body, including the heart, bones, joints, respiratory system and central nervous system, leading to a shortened lifespan.
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The Web Diva for the Accessible Techcomm website since 2012. Fellow of the Society for Technical Communication. STC member since June 1979. A founder and former webmaster for the STC Special Needs Committee, which became the STC AccessAbility SIG (2001-2011).