There is no specific treatment available for Sanfilippo syndrome. Experiments in animal models suggest that enzyme replacement may be used for treatment in the future.
Support Groups:
Additional information and resources are available from the National MPS Society.
Severe retardation is the most important of the clinical problems. IQs may be below 50. Severe cases lead to death before 20 years of age.
In a minority of cases, Sanfilippo is compatible with a normal lifespan. The affected person may develop retinal degeneration leading to blindness, or may have seizures.
Complications:
Blindness
Seizures
Mental retardation
Progressive neurologic disease leading to becoming wheelchair bound
Inability to care for self
Calling your health care provider:
Call your health care provider if your child does not seem to be growing or developing normally.
Call for an appointment with your health care provider if you plan to have children and you have a family history of Sanfilippo syndrome.
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