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A Rare Case of Mucopolysaccharidosis: Hunter Syndrome
Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a member of a group of inherited metabolic disorders together termed mucopolysaccharidosis (MPSs). It is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase. The prevalence of this syndrome is 1...
Uloženo v:
| Vydáno v: | J Clin Diagn Res |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
JCDR Research and Publications (P) Limited
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4437174/ https://ncbi.nlm.nih.gov/pubmed/26023658 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2015/13251.5858 |
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