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Effects of enzyme replacement therapy on growth in patients with mucopolysaccharidosis type II
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is an X-linked, recessive, lysosomal storage disorder caused by deficiency of iduronate-2-sulfatase. It has multisystemic involvement, with manifestations in the brain, upper respiratory tract, heart, abdomen, joints and bones. Bone involvement...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Springer Netherlands
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3026660/ https://ncbi.nlm.nih.gov/pubmed/20978944 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-010-9215-2 |
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