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Congenital Disorder

Mucopolysaccharidosis III

AMW:DIS:160098

Mucopolysaccharidosis characterized by HEPARAN 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.

Pathology clinical

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