Glycogen Storage Diseases Types I-VII: eMedicine Dermatology
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Glycogen Storage Diseases Types I-VII: eMedicine Dermatology
View full resource at emedicine.medscape.com
Tags: Dermatology, Disease and Condition
Most Recently Shared on April 21, 2010 at 8:08 pm By:
Glycogen storage diseases occur due to the body's inability to break down or use glycogen. Learn about these diseases.http://bit.ly/dekuIN
Mucopolysaccharidoses Types I-VII: eMedicine Dermatology
emedicine.medscape.com — “Overview: Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases, each of which is produced by an inherited deficiency of an enzyme involved in the degradation of acid mucopolysaccharides, now called glycosaminoglycans (GAGs). These diseases are autosomal ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 10:43 pm By:
Susan Scroggins Active Health Library and Health Advocate
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases. Learn about each type. http://bit.ly/b5hw00
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