glycogen storage disease emedicine
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Glycogen-Storage Disease Type I: eMedicine Pediatrics: Genetics and .
Overview: In 1929, von Gierke provided the initial description of glycogen-storage disease type I (GSD I) from autopsy reports of 2 children whose large livers .　->
Glycogen Storage Disease, Type Ia: eMedicine Endocrinology
Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. . Endocrinology > Metabolic Disorders. Glycogen Storage Disease, Type Ia .　->
Glycogen storage disease - Wikipedia, the free encyclopedia
Type I Glycogen Storage Disease accounts for about 25% of all cases of GSD . GSD Type I from emedicine. American Liver Foundation information on Type I .　->
Association for Glycogen Storage Disease, USA
In Type VI Glycogen Storage Disease (GSD VI), the most frequent first symptoms . Type VI GSD info from eMedicine. Hers Disease from Madisons Foundation .　->
Glycogen storage disease: Definition from Answers.com
. One of several inborn errors in the metabolism of glycogen, classified on the basis of the enzyme . b "eMedicine - Glycogen-Storage Disease Type VI : .　->
Glycogen storage disease type II: Definition from Answers.com
. resulting in the accumulation of glycogen in all organs and marked by . "eMedicine - Glycogen-Storage Disease Type II : Article by Jennifer Ibrahim" .　->
eMedicine Search
Search across eMedicine's collection of over 6,500 clinical review articles . EMEDICINE RESULTS. 21 documents matched Glycogen storage muscle disease Pompe .　->
CIGNA - Glycogen Storage Disease Type V
Wasserstein M. Glycogen Storage Disease Type V. eMedicine. Last Updated: . www.emedicine.com/med/topic911.htm. GLYCOGEN STORAGE DISEASE (GSD) TYPE V and VII. .　->
