Orthopedic manifestations in patients with mucopolysaccharidosis type II (Hunter syndrome) enrolled in the Hunter Outcome Survey

Mucopolysaccharidosis type II (MPS II or Hunter syndrome) is a rare, inherited disorder caused by deficiency of the lysosomal enzyme iduronate-2-sulfatase. As a result of this deficiency, glycosaminoglycans accumulate in lysosomes in many tissues, leading to progressive multisystemic disease. The ca...

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Detalles Bibliográficos
Autores principales: Link, Bianca, de Camargo Pinto, Louise Lapagesse, Giugliani, Roberto, Wraith, James Edmond, Guffon, Nathalie, Eich, Elke, Beck, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143973/
https://www.ncbi.nlm.nih.gov/pubmed/21808707
http://dx.doi.org/10.4081/or.2010.e16

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3143973/
https://www.ncbi.nlm.nih.gov/pubmed/21808707
http://dx.doi.org/10.4081/or.2010.e16

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