Glycogen Storage Disease Type II

Glycogen Storage Disease Type II Websites

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.- Category ID : 76399

List of Glycogen_Storage_Disease_Type_II Sites 3 Websites

United POMPE Foundation

Pompe Disease support group. Assisting families with unmet medical costs.

Pompe.com

For individuals and families who are living with Pompe disease, and for the health care professionals who treat them. From Genzyme Corporation.

eMedicine

Glycogen Storage Disease Type II : Article by Jennifer Ibrahim, MD.

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