Explore: Glycogen Storage Disease Type II, Brain Diseases
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....
This page was last updated on September 7th, 2008
This page was last updated on September 7th, 2008
Glycogen Storage Disease Type II (from Brain Diseases)
Canadian Content » Health » Conditions_and_Diseases » Neurological_Disorders » Brain_Diseases » Glycogen_Storage_Disease_Type_II »
United POMPE Foundation
Pompe Disease support group. Assisting families with unmet medical costs.
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.
Acid Maltase Deficiency
A brief summary of AMD along with links and news.
Pompe Disease support group. Assisting families with unmet medical costs.
Kevin O'Donnell's Web site. Father of an affected child provides information about this glycogen storage disease.
Glycogen Storage Disease Type II : Article by Jennifer Ibrahim, MD.
A brief summary of AMD along with links and news.
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