Glycogen Storage Disease Type II Brain Diseases Neurological Disorders

Glycogen Storage Disease Type II Brain Diseases Neurological Disorders

An autosomal recessively inherited glycogen storage disease caused by glucan 1,4-Alpa-Glucosidase Definciency. Large amounts of glycogen accumulate in the lysomes of skeletal muscle ( muscle, skeletal); heart; liver; spinal cord; and brain.

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See Also:

Pompe.com - For individuals and families who are living with Pompe disease, and for the health care professionals who treat them. From Genzyme Corporation.
Pompe's Disease Page - Kevin O'Donnell's Web site. Father of an affected child provides information about this glycogen storage disease.
eMedicine - Glycogen Storage Disease Type II : Article by Jennifer Ibrahim, MD.
United POMPE Foundation - Pompe Disease support group. Assisting families with unmet medical costs.

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