Mucopolysaccharidosis I


Disease, Hurler's


Gargoylism, Hurler Syndrome


Hurler Disease

Hurler Scheie Syndrome

Hurler Syndrome

Hurler Syndrome Gargoylism

Hurler's Disease

Hurler's Syndrome

Hurler-Scheie Syndrome



Mucopolysaccharidosis 1

Mucopolysaccharidosis 5

Mucopolysaccharidosis I S

Mucopolysaccharidosis I-S

Mucopolysaccharidosis Is

Mucopolysaccharidosis Type I

Mucopolysaccharidosis Type Ih

Mucopolysaccharidosis Type Ih S

Mucopolysaccharidosis Type Ihs

Mucopolysaccharidosis Type Is

Mucopolysaccharidosis V

Pfaundler-Hurler Syndrome

Scheie Syndrome

Scheie's Syndrome

Syndrome, Hurler's

Syndrome, Scheie's

Type Ih, Mucopolysaccharidosis

Type Ihs, Mucopolysaccharidosis

alpha L Iduronidase Deficiency

alpha-L-Iduronidase Deficiencies

alpha-L-Iduronidase Deficiency

Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM; hepatosplenomegaly; thick, coarse facial features with low nasal bridge; corneal clouding; cardiac complications; and noisy breathing.