The clinical profiles of female patients with Fabry disease in Latin America: A Fabry Registry analysis of natural history data from 169 patients based on enzyme replacement therapy status

BACKGROUND: Fabry disease is an X‐linked lysosomal storage disorder with heterogeneous clinical expression in female patients ranging from asymptomatic to severe clinical presentations as in classic males. We assessed clinical profiles and compared natural history data of female patients eventually...

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Detalles Bibliográficos
Autores principales: Martins, Ana M., Cabrera, Gustavo, Molt, Fernando, Suárez‐Obando, Fernando, Valdés, Régulo A., Varas, Carmen, Yang, Meng, Politei, Juan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Research Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718114/
https://www.ncbi.nlm.nih.gov/pubmed/31497488
http://dx.doi.org/10.1002/jmd2.12071

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718114/
https://www.ncbi.nlm.nih.gov/pubmed/31497488
http://dx.doi.org/10.1002/jmd2.12071

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