Glycogen Storage Disease, Type II (Pompe Disease): eMedicine Endocrinology
Links shared publicly online about this topic.
- 1,190total visits
Glycogen Storage Disease, Type II (Pompe Disease): eMedicine Endocrinology
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
Tags: Endocrinology, Disease and Condition
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
Advertisement
