Hurler syndrome, also called mucopolysaccharidosis type I, is an inherited disease in which the body lacks an enzyme called alpha-L-iduronidase. Without this enzyme, the body cannot properly break down long chains of sugar molecules called glycosaminoglycans. As a result, these molecules accumulate in the body, causing numerous health problems. Children with Hurler syndrome typically die before the age of 10, but may live longer with treatment.
Children with the disease appear normal at birth, but around the age of 9 months they typically begin developing some or all of the following symptoms:
A milder form of mucopolysaccharidosis type I is known as Scheie syndrome, and an intermediate form is known as Hurler-Scheie syndrome.
Approximately 1 in 100,000 people have Hurler syndrome. It has been found in people of all ethnicities.
Depending on the severity of Hurler syndrome and the age of the child, one of several treatments may prevent or ameliorate some symptoms of the disease.
Bone marrow transplants can be effective in relieving physical aspects of Hurler syndrome, although it does not seem to help the bone or eye symptoms. Children who receive bone marrow transplants early—before the age of 2—tend to have better mental development, although they still have learning problems and progressive mental decline. Outcomes of the procedure do vary, but a bone marrow transplant can prolong the lifespan of a person with Hurler syndrome, even though it will still be significantly shortened. Note that the procedure itself carries a high risk of fatality.
Umbilical cord blood is a more recent treatment for Hurler syndrome, allowing for an unrelated donor and eliminating the need for total body radiation, as is the norm with a bone marrow transplant. This treatment can prolong the lifespan of an affected child, but also does not help the bone and eye issues. A cord blood transplant can help prevent a certain measure of mental decline if it is performed before significant damage is done to the intellect, often before the age of 18 months. Like bone marrow transplants, the procedure itself carries a high risk of fatality and can result in a variety of outcomes.
Enzyme replacement therapy using recombinant human alpha-L-iduronidase (brand name: Aldurazyme) has also been shown to benefit people with Hurler syndrome, relieving many of the physical symptoms. Enzyme replacement may be used in tandem with the above surgical options. This treatment is relatively new and further study is needed to determine its long-term success.
Other symptoms of the disease can be addressed as they arise. Examples of these treatments include special education for developmental delays, heart valve replacement, shunting to remove excess fluid and relieve pressure from around the brain, sunglasses or hats to promote better vision, and physical therapy to aid in movement.
The prognosis for people with Hurler syndrome is generally poor. They need special education and assistance to perform ordinary daily functions, and are often wheelchair-bound. Death usually occurs within the first 10 years of life, although early treatment such as a bone marrow transplant can extend the lifespan. Heart and breathing problems are often the cause of death among children with the disease.
A Canadian non-profit with similar goals and aims to its American counterpart, the National MPS Society.
PO Box 30034
North Vancouver, British Columbia V7H 2Y8 Canada
Phone: (604) 924-5130
Secondary Phone: (800) 667-1846
An online medical encyclopedia written using information from the U.S. National Library of Medicine, the National Institutes of Health, and other government agencies and health-related organizations.