Beschreibung:
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.
Synonym(s):
Polydystrophische Oligophrenie /
Sanfilippo-Krankheit /