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Results 1 - 10 of 20 for Glycogen storage disease type 4
  1. ... 4 glycogenosis, type IV glycogen storage disease IV glycogen storage disease type 4 GSD4 GSD IV GSD type IV type IV ...
  2. ... research PubMed - Recent literature OMIM - Genetic disorder catalog (4 links) What other names do people use for glycogen storage disease type IX? GSDIX GSD IX PhK deficiency phosphorylase b ...
  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. ... V? You may find the following resources about glycogen storage disease type V helpful. These materials are written for the general public. MedlinePlus - Health information (4 links) Genetic and Rare Diseases Information Center - Information ...
  5. Type I Glycogen Storage Disease (American Liver Foundation)  
    ... when a person is not eating. How is type I glycogen storage disease diagnosed? Children with GSD I are usually diagnosed between 4 and 10 months of age. Testing will most ...
  6. Genetics Home Reference: Pompe disease From the National Institutes of Health (National Library of Medicine)  
    ... maltase deficiency acid maltase deficiency disease alpha-1,4-glucosidase deficiency AMD deficiency of alpha-glucosidase GAA deficiency glycogenosis Type II glycogen storage disease type II GSD2 GSD II Pompe's disease For ...
  7. G6PD Deficiency (Chicago Center for Jewish Genetic Disorders)  
    ... Traits Beta Thalassemia Familial Mediterranean Fever G6PD Deficiency Glycogen Storage Disease, Type III Wolman Disease Personal Story G6PD Deficiency Quick Facts Disease Frequency: 400 million people worldwide Carrier Frequency: 1 in 4 to1 in 20 in tropical Africa, the Middle ...
  8. ... Professionals What glossary definitions help with understanding glycogen storage disease type VI? acidosis ; autosomal ; ... (4 links) The resources on this site should not ...
  9. ... What is glycogen storage disease type I? Glycogen storage disease ... around the age of 3 or 4 months, when babies start to sleep through the ...
  10. ... to their condition. It is unclear why this type of enzyme deficiency does not cause any health problems. Read more ... and Rare Diseases Information Center - Information ...
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