Mucopolysaccharidosis II


Deficiency, I2S

Deficiency, Iduronate 2-Sulfatase

Deficiency, Iduronate Sulfatase

Deficiency, Sulfoiduronate Sulfatase

Gargoylism, Hunter Syndrome

Hunter Syndrome

Hunter Syndrome Gargoylism

Hunter's Syndrome

Hunters Syndrome

I2S Deficiency

Iduronate 2 Sulfatase Deficiency

Iduronate 2-Sulfatase Deficiency

Iduronate Sulfatase Deficiency

Mucopolysaccharidosis 2

Mucopolysaccharidosis Type 2

Mucopolysaccharidosis Type II

Sulfoiduronate Sulfatase Deficiency

Syndrome, Hunter

Syndrome, Hunter's

Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.