Anderson–Fabry Disease: From Endothelial Dysfunction to Emerging Therapies

The Anderson–Fabry disease is a rare, X-linked, multisystemic, progressive lysosomal storage disease caused by α-galactosidase A total or partial deficiency. The resulting syndrome is mainly characterized by early-onset autonomic neuropathy and life-threatening multiorgan involvement, including rena...

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Detalles Bibliográficos
Autores principales: Stamerra, Cosimo A., Del Pinto, Rita, di Giosia, Paolo, Ferri, Claudio, Sahebkar, Amirhossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8137293/
https://www.ncbi.nlm.nih.gov/pubmed/34095851
http://dx.doi.org/10.1155/2021/5548445

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8137293/
https://www.ncbi.nlm.nih.gov/pubmed/34095851
http://dx.doi.org/10.1155/2021/5548445

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