No differences in native T1 of the renal cortex between Fabry disease patients and healthy subjects in cardiac-dedicated native T1 maps

No differences in native T1 of the renal cortex between Fabry disease patients and healthy subjects in cardiac-dedicated native T1 maps

ABSTRACT: Background: Fabry disease (FD) is an X-linked inherited lysosomal storage disease that is caused by deficient activity of the enzyme alpha-galactosidase A. Cardiovascular magnetic resonance (CMR) imaging can detect cardiac sphingolipid accumulation using native T1 mapping. The kidneys are...

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Bibliographic Details
Main Authors: Anna Damlin, Felix Kjellberg, Raquel Themudo, Kelvin Chow, Henrik Engblom, Mikael Oscarson, Jannike Nickander
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Journal of Cardiovascular Magnetic Resonance
Subjects:
Fabry disease
Lysosomal storage diseases
Magnetic resonance imaging
Kidney failure
Online Access:http://www.sciencedirect.com/science/article/pii/S1097664724011311
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