The severe form of this disorder can lead to Hurler syndrome.

Hurler syndrome is inherited, which means that your parents must pass the disease on to you.

Symptoms of Hurler syndrome most often appear between ages 3 and 8.

However, this medication is not a cure for Hurler syndrome.

Both parents need to pass down the faulty gene in order for you to develop Hurler syndrome.

Hurler syndrome is a disease with a poor outlook.

Laronidase may improve breathing and walking ability in people with Hurler syndrome.

Infants with severe Hurler syndrome appear normal at birth.

Experts recommend genetic counseling and testing for couples with a family history of Hurler syndrome who are considering having children.

Hurler syndrome was once known as "Gargoylism"

Laronidase is used to treat some of the symptoms of a genetic condition called Hurler syndrome.

Hurler syndrome is a metabolic disorder in which the body lacks the enzyme needed to break down certain sugars and proteins.

Persons with Hurler syndrome do not make a substance called lysosomal alpha-L-iduronidase.

The symptoms of I-cell disease are similar to but more severe than those of Hurler syndrome.

Hurler syndrome belongs to a group of diseases called mucopolysaccharidoses, or MPS.

Children with Hurler syndrome often die before age 10 from obstructive airway disease, respiratory infections, or cardiac complications.

A medical example is a heterokaryon composed of nuclei from Hurler syndrome and Hunter syndrome.

Children with Maroteaux-Lamy syndrome, usually have normal intellectual development but share many of the physical symptoms found in Hurler syndrome.

Hunter syndrome is X-linked while Hurler syndrome is autosomal recessive.

Hurler syndrome is often classified as a lysosomal storage disease, and is clinically related to Hunter Syndrome.

The purpose of this registry is to track the progression of this disorder and the effects that laronidase has on long-term treatment of Hurler syndrome.

She also wrote autobiographical works that addressed the death of Frank, her husband who died of cancer, and the story of their son suffering from Hurler syndrome.

Hurler syndrome is a rare, inherited disease of metabolism in which a person cannot break down long chains of sugar molecules called glycosaminoglycans (formerly called mucopolysaccharides).

ML II is a particularly severe form of ML that resembles one of the mucopolysaccharidoses called Hurler syndrome.

Because Hurler syndrome is an autosomal recessive disorder, affected persons have two non-working copies of the IDUA gene.

Hurler syndrome was once known as "Gargoylism"

Gangliosidosis GM1 Type 1 Gangliosidosis GM2 Type 2 Ganser Syndrome Gardner Syndrome Gargoylism Garies-Mason Syndrome Gas (Flatus) Gasser Syndrome Gastric cancer: Prevention - Health Prof..