Glycogen Storage Disease, Type IV: eMedicine Endocrinology
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Glycogen Storage Disease, Type IV: eMedicine Endocrinology
View full resource at emedicine.medscape.com
Tags: Endocrinology, Disease and Condition
Most Recently Shared on May 5, 2010 at 7:03 pm By:
Type IV glycogen storage disease is also known as Andersen disease, and is a result of transglucosidase deficiency. http://bit.ly/boizB9
Glycogen Storage Disease, Type VII: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:08 pm By:
Type VII glycogen storage disease is also called Tarui disease and is due to phosphofructokinase deficiency. Learn more.http://bit.ly/d8jUrn
Glycogen Storage Disease, Type VI: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:06 pm By:
Hers disease, also called type VI glycogen storage disease, is characterized by phosphorylase deficiency. http://bit.ly/aBvj7k
Glycogen Storage Disease, Type V: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:04 pm By:
McArdle disease, or type V glycogen storage disease is myophosphorylase deficiency. Learn more. http://bit.ly/cPhOaH
Glycogen Storage Disease, Type III: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) results from the absence of enzymes that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the defect has systemic consequences, but, in ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:02 pm By:
Type III glycogen storage disease is also called Forbes-Cori disease, & is a result of debranching enzyme deficiecy. http://bit.ly/aGgc9e
Glycogen Storage Disease, Type II (Pompe Disease): eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to monosaccharides, of which glucose is the predominant component. Enzyme deficiency results in glycogen ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 7:01 pm By:
Type II glycogen storage disease, or Pompe disease, is a result of acid maltase deficiency. More about type II GSD. http://bit.ly/bQYTVx
Glycogen Storage Disease, Type Ib: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 6:59 pm By:
Unfortunately, no specific treatment or cure exists for type Ib glycogen storage disease. Learn symptoms. http://bit.ly/cDomLM
Glycogen Storage Disease, Type Ia: eMedicine Endocrinology
emedicine.medscape.com — “Overview: A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation in tissues. In many cases, the ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 6:58 pm By:
Type Ia glycogen storage disease can cause seizures or cardiomegaly. Learn more specifics. http://bit.ly/9dAIVV
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