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Enzyme replacement therapy for Anderson‐Fabry disease
BACKGROUND: Anderson‐Fabry disease is an X‐linked defect of glycosphingolipid metabolism. Progressive renal insufficiency is a major source of morbidity, additional complications result from cardio‐ and cerebro‐vascular involvement. Survival is reduced among affected males and symptomatic female car...
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| Publicado no: | Cochrane Database Syst Rev |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley & Sons, Ltd
2016
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6481759/ https://ncbi.nlm.nih.gov/pubmed/27454104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD006663.pub4 |
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