Directory of Glycogen Storage Disease Type II Resources

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.

Resources in This Category

• eMedicine

  http://emedicine.medscape.com/article/947870-overview
  Glycogen Storage Disease Type II : Article by Jennifer Ibrahim, MD.

• Pompe's Disease Page

  http://www.pompe.org.uk/
  Kevin O'Donnell's Web site. Father of an affected child provides information about this glycogen storage disease.

• Pompe.com

  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.

• United POMPE Foundation

  http://www.unitedpompe.com/
  Pompe Disease support group. Assisting families with unmet medical costs.

Related Categories

• Home > Health > Conditions and Diseases > Chronic Illness
• Home > Health > Conditions and Diseases > Genetic Disorders
• Home > Health > Conditions and Diseases > Nutritional and Metabolic Disorders

 

Home > Health > Conditions and Diseases > Neurological Disorders > Brain Diseases > Glycogen Storage Disease Type II

 

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