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