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...
Main Authors: | Giovanni Donato Aquaro, Carmelo De Gori, Lorenzo Faggioni, Maria Luisa Parisella, Giacomo Aringhieri, Dania Cioni, Riccardo Lencioni, Emanuele Neri |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-11-01
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Series: | Diagnostics |
Subjects: | |
Online Access: | https://www.mdpi.com/2075-4418/12/11/2652 |
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