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Results 1 - 4 of 4 for Deficiency of "alpha-glucosidase"
  1. Genetics Home Reference: Pompe disease From the National Institutes of Health (National Library of Medicine)  
    ... deficiency disease alpha-1,4-glucosidase deficiency AMD deficiency of alpha-glucosidase GAA deficiency glycogenosis Type II glycogen storage disease type II ...
  2. Understanding Pompe Disease From the National Institutes of Health (National Institute of Arthritis and Musculoskeletal and Skin Diseases)  
    ... Disease? Pompe (POM-pay) disease, also known as glycogen storage disease type II or acid maltase deficiency, is a rare genetic disorder that results in profound muscle weakness. The disease is caused by ... excessive amounts of glycogen to accumulate in the body’s tissues, which ...
  3. Metabolic Diseases of Muscle (Muscular Dystrophy Association) - PDF  
    ... CARbohydRAtE-PRoCEssing disoRdERs These disorders affect the breakdown ... Pompe disease, lysosomal storage disease Onset: Infancy ...
  4. Pompe Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    ... Synonym(s): Neurological Manifestations of Pompe Disease, Acid Maltase Deficiency, Glycogen ... makes an enzyme called acid alpha-glucosidase (GAA). Normally, the body uses GAA to break ...