Significance of NT-proBNP and High-sensitivity Troponin in Friedreich Ataxia

Significance of NT-proBNP and High-sensitivity Troponin in Friedreich Ataxia

Background: Friedreich’s ataxia (FA) is a rare autosomal recessive mitochondrial disease resulting of a triplet repeat expansion guanine-adenine-adenine (GAA) in the frataxin (FXN) gene, exhibiting progressive cerebellar ataxia, diabetes and cardiomyopathy. We aimed to determine the relationship bet...

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Bibliographic Details
Main Authors: Lise Legrand, Carole Maupain, Marie-Lorraine Monin, Claire Ewenczyk, Richard Isnard, Rana Alkouri, Alexandra Durr, Francoise Pousset
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Journal of Clinical Medicine
Subjects:
Friedreich ataxia
hs troponin
NT-proBNP
cardiomyopathy
Online Access:https://www.mdpi.com/2077-0383/9/6/1630

Internet

https://www.mdpi.com/2077-0383/9/6/1630

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