Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) are a group of rare, inherited metabolic disorders where the body is unable to properly break down long chains of sugars called glycosaminoglycans (GAGs). This leads to a buildup of these GAGs in various parts of the body, such as the skeleton, skin, and other organs. Symptoms of MPS vary greatly and can include skeletal deformities, organ failure, and developmental delays. There is no cure for MPS, but treatments are available that can improve the quality of life and reduce the progression of the disease. These treatments focus on managing the signs and symptoms of the disorder and can include enzyme replacement therapy, physical therapy, and occupational therapy. Improving awareness of MPS and its associated treatments is critical in order to ensure that patients diagnosed with the disorder receive the best possible care available.