Loss of function: This is a very rare disease, inherited when both parents are usually carriers. Because of the deficient enzyme, arylsulfatase a, patients suffer from a gradual destruction of myelin sheath, the protective covering of nerves. At the end, loss of muscle function, seizures, possibly coma, and mental illness (in older people) prevail. Unfortunately, no cure, though therapies may improve life quality.
Answered 3/26/2013
5.7k views
A doctor has provided 1 answer
90,000 U.S. doctors in 147 specialties are here to answer your questions or offer you advice, prescriptions, and more.
Ask your question