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Case report: An unusual case of desmin myopathy associated with heart failure and arrhythmia
INTRODUCTION: Desmin myopathy is a novel desmin (DES) indel mutation that causes severe atypical cardiomyopathy as well as atrioventricular block and skeletal myopathy. The mutation of the gene of the nodal tail causes myocardial injury. Rarely does desmin myopathy cause bilateral ventricular change...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9357943/ https://www.ncbi.nlm.nih.gov/pubmed/35958417 http://dx.doi.org/10.3389/fcvm.2022.944459 |