Mucopolysaccharidoses Types I-VII: eMedicine Dermatology
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Mucopolysaccharidoses Types I-VII: eMedicine Dermatology
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 ...
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Tags: Dermatology, Disease and Condition
Most Recently Shared on April 21, 2010 at 10:43 pm By:
Mucopolysaccharidoses (MPSs) are a group of lysosomal storage diseases. Learn about each type. http://bit.ly/b5hw00
Glycogen Storage Diseases Types I-VII: eMedicine Dermatology
emedicine.medscape.com — “Overview: Glycogen storage disease type IGlycogen storage disease (GSD) type I is also known as von Gierke disease or hepatorenal glycogenosis. von Gierke1 described the first patient with GSD type I in 1929 under the name ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 8:08 pm By:
Susan Scroggins Active Health Library and Health Advocate
Glycogen storage diseases occur due to the body's inability to break down or use glycogen. Learn about these diseases.http://bit.ly/dekuIN
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