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Results 1 - 6 of 6 for Glycogen storage "disease," type II
  1. Genetics Home Reference: Pompe disease From the National Institutes of Health (National Library of Medicine)  
    ... include treatment providers. Baby's First Test Gene Review: Glycogen Storage Disease Type II (Pompe Disease) Genetic Testing Registry: Glycogen storage disease, ...
  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 ... to break down glycogen (stored sugar) into glucose (sugar). But in Pompe ...
  3. Metabolic Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
  4. ... of the following conditions: Biliary cirrhosis . Alagille syndrome . Glycogen storage disease . Progressive familial intrahepatic disease . Tyrosinemia . Patients with tyrosinemia ...
  5. Chromium From the National Institutes of Health (National Institutes of Health, Office of Dietary Supplements)  
    ... 872 patients — implications for the prevention of cardiovascular disease and type II diabetes mellitus. Metabolism 1997;46:469-73. Gibson RS. Principles of Nutritional Assessment, 2nd Edition. Oxford University Press, New ... Nutrition in Health and Disease, 9th Edition (edited by Shils ME, Olson JA, ...
  6. ... at any age, even during childhood. A progressive disease, type 2 diabetes usually begins with insulin resistance , a ... tissue that it believes to be foreign. In type 1 diabetes, an autoimmune disease, the immune system attacks and destroys the insulin- ...