Diagnosis and follow-up of patients with Hunter syndrome in Spain: A Delphi consensus

Hunter syndrome or mucopolysaccharidosis type II (MPSII) is a progressive multisystem X-linked lysosomal storage disease caused by mutations in the IDS gene that shows a wide spectrum of clinical symptoms and severity. Idursulfase, a specific enzyme replacement therapy (ERT) for MPSII, has been avai...

Descripción completa

Detalles Bibliográficos
Autores principales: González-Gutiérrez-Solana, Luis, Guillén-Navarro, Encarnación, del Toro, Mireia, Dalmau, Jaime, González-Meneses, Antonio, Couce, María L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086518/
https://www.ncbi.nlm.nih.gov/pubmed/30024503
http://dx.doi.org/10.1097/MD.0000000000011246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086518/
https://www.ncbi.nlm.nih.gov/pubmed/30024503
http://dx.doi.org/10.1097/MD.0000000000011246

Ejemplares similares