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Mucopolysaccharidosis III

Polydystrophic Oligophrenia | Sanfilippo' | s Syndrome | MPS III A | MPS III B | MPS III C | MPS III D | Mucopolysaccharidosis 3 | San Filippo' | s Syndrome | IIIs, Mucopolysaccharidosis | Mucopolysaccharidosis IIIs | San Filippo Syndrome

Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme.
 
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