Fabry disease – current data and therapeutic approaches

Fabry disease represents an X-linked inherited disorder resulting in the accumulation of globotriaosylceramide (Gb3). This review explains the clinical manifestations and the possible therapies for this condition. Fabry disease is considered the second most frequent lysosomal storage disease. More t...

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Detalles Bibliográficos
Autores principales: Dinu, Ilie-Robert, Firu, Ştefan-George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597377/
https://www.ncbi.nlm.nih.gov/pubmed/34609404
http://dx.doi.org/10.47162/RJME.62.1.01

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597377/
https://www.ncbi.nlm.nih.gov/pubmed/34609404
http://dx.doi.org/10.47162/RJME.62.1.01

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