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![]() ![]() Which are the Mucopolysaccharide Diseases?
These rare lysosomal storage diseases are refered to as MPS I-VII or more commonly by the name of the doctor who first described the condition. These commonly include:
MPS I - Hurler, Hurler Scheie and Scheie Included also are the Mucolipidoses, other 'storage diseases' and the following conditions which are similar to Mucopolysaccharide Diseases: ML I - Neuramidase Deficiency
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