Cardiac Magnetic Resonance in Fabry Disease: Morphological, Functional, and Tissue Features

Fabry disease (FD) is an X-linked inheritable storage disease caused by a deficiency of alpha-galactosidase causing lysosomal overload of sphingolipids. FD cardiomyopathy is characterized by left ventricular (LV) hypertrophy and should be considered in differential diagnosis with all the other cause...

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Detalles Bibliográficos
Autores principales: Aquaro, Giovanni Donato, De Gori, Carmelo, Faggioni, Lorenzo, Parisella, Maria Luisa, Aringhieri, Giacomo, Cioni, Dania, Lencioni, Riccardo, Neri, Emanuele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689455/
https://www.ncbi.nlm.nih.gov/pubmed/36359495
http://dx.doi.org/10.3390/diagnostics12112652

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689455/
https://www.ncbi.nlm.nih.gov/pubmed/36359495
http://dx.doi.org/10.3390/diagnostics12112652

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