What is another name for Hurler Syndrome?

Hurler Syndrome is also known as Mucopolysaccharidosis Type I. This condition is a genetic disorder caused by the deficiency of the enzyme alpha-L-iduronidase, which leads to the accumulation of glycosaminoglycans (GAGs) in the body. The buildup of these substances affects various systems and leads to a range of symptoms, including developmental delays, skeletal abnormalities, and organ enlargement.

Mucopolysaccharidosis refers to a group of inherited metabolic disorders caused by the body's inability to properly break down GAGs. Since Hurler Syndrome falls under this category, the name Mucopolysaccharidosis Type I accurately reflects both the specific type of disorder and its metabolic nature. This name distinction is important for classification and understanding the underlying pathology associated with the disorder.