Home > Health > Conditions and Diseases > Neurological Disorders > Brain Diseases > Glycogen Storage Disease Type II
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.
http://emedicine.medscape.com/article/947870-overview
Glycogen Storage Disease Type II : Article by Jennifer Ibrahim, MD.
http://www.pompe.org.uk/
Kevin O'Donnell's Web site. Father of an affected child provides information about this glycogen storage disease.
http://www.pompe.com/
For individuals and families who are living with Pompe disease, and for the health care professionals who treat them. From Genzyme Corporation.
http://www.unitedpompe.com/
Pompe Disease support group. Assisting families with unmet medical costs.
Home > Health > Conditions and Diseases > Neurological Disorders > Brain Diseases > Glycogen Storage Disease Type II
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