Health Conditions and Diseases Nutritional and Metabolic Disorders Inherited
Mucopolysaccharidoses
5
Mucopolysaccharides are long molecular chains of sugar. They are used by the body in the building of connective tissues. They must also be broken down and reused by the body. Children with MPS are unable to produce one of the enzymes essential to this task.
Mucopolysaccharide diseases (or Mucopolysaccharidosis or MPS) are genetic diseases caused by recessive genes.
There are seven Mucopolysaccharide (MPS) disorders. They are referred to as MPS I-VII but many of them go by the name of the doctor who first described the condition as well.
Hunter syndrome, Hurler syndrome, Scheie syndrome, Sanfilippo syndrome, Maroteaux-Lamy syndrome, and Morquio disease are all Mucopolysaccharide diseases.
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Founded to provide information and support to affected individuals and their families.
Non-profit organization advocating for families affected by mucopolysaccharide and related diseases. Located in Durham, North Carolina, USA.
Offers a list of synonyms, a general discussion and further resources.
A voluntary support group in the UK which represents children and adults suffering from Mucopolysaccharide and Related Lysosomal Storage Diseases, their families, carers and professionals.
A voluntary support group in the UK which represents children and adults suffering from Mucopolysaccharide and Related Lysosomal Storage Diseases, their families, carers and professionals.
Non-profit organization advocating for families affected by mucopolysaccharide and related diseases. Located in Durham, North Carolina, USA.
Founded to provide information and support to affected individuals and their families.
Offers a list of synonyms, a general discussion and further resources.
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Last update:
March 12, 2020 at 5:25:03 UTC
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- Recently edited by shedragon
- Recently edited by shedragon