Cardiac Imaging in Anderson-Fabry Disease: Past, Present and Future

Anderson-Fabrydisease is an X-linked lysosomal storage disorder caused by a deficiency in the lysosomal enzyme α-galactosidase A. This results in pathological accumulation of glycosphingolipids in several tissues and multi-organ progressive dysfunction. The typical clinical phenotype of Anderson-Fab...

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Detalles Bibliográficos
Publicado en:J Clin Med
Main Authors: Esposito, Roberta, Santoro, Ciro, Mandoli, Giulia Elena, Cuomo, Vittoria, Sorrentino, Regina, La Mura, Lucia, Pastore, Maria Concetta, Bandera, Francesco, D’Ascenzi, Flavio, Malagoli, Alessandro, Benfari, Giovanni, D’Andrea, Antonello, Cameli, Matteo
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2021
Assuntos:
Review
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC8124634/
https://ncbi.nlm.nih.gov/pubmed/34066467
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm10091994
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