Other names: Hurler Syndrome
Mucopolysaccharidosis Type I is a condition of varying severity that affects many parts of the body. It may be characterized by severe abnormality in development of skeletal cartilage and bone, with dwarfism, kyphosis, deformed limbs, limitation of joint motion, spadelike hands, corneal clouding, hepatosplenomegaly, mental retardation, and gargoylelike facies.
Drugs used to treat Mucopolysaccharidosis Type I
| Name | Drug Class |
|---|---|
| Laronidase | Lysosomal enzymes |
| Aldurazyme | Lysosomal enzymes |
