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Diagnosis and follow-up of patients with Hunter syndrome in Spain

  • Published:2018-07 Issue:29 Volume:97 Page:e11246
  • ISSN:0025-7974
  • Container-title:Medicine
  • language:en
  • Short-container-title:

Author:

González-Gutiérrez-Solana Luis,Guillén-Navarro Encarnación,del Toro Mireia,Dalmau Jaime,González-Meneses Antonio,Couce María L.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference40 articles.

1. Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy;Wraith;Eur J Pediatr,2008

2. Enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II (Hunter syndrome);Da Silva;Cochrane Database Syst Rev,2014

3. Clinical practice guideline for the management of Hunter syndrome. Hunter España working group;Guillén-Navarro;Med Clin (Barc,2013

4. Hunter Syndrome European Expert Council. Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease;Scarpa;Orphanet J Rare Dis,2011

5. Clinical manifestations in female carriers of mucopolysaccharidosis type II: a Spanish cross-sectional study;Guillén-Navarro;Orphanet J Rare Dis,2013

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