Mucopolysaccharidosis Type II: eMedicine Pediatrics: Genetics and Metabolic Disease
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Mucopolysaccharidosis Type II: eMedicine Pediatrics: Genetics and Metabolic Disease
Overview: Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a member of a group of inherited metabolic disorders collectively termed mucopolysaccharidoses (MPSs). The MPSs are caused by a deficiency of lysosomal enzymes required for the degradation ...
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Tags: Genetic, Metabolic, Disease and Condition, Children's Health
Most Recently Shared on July 15, 2009 at 9:36 pm By:
Mucopolysaccharidosis Type II article over at eMedicine has been updated. http://bit.ly/VTYYW #genetics #pediatrics #health #medicine
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