Subclinical myocardial injury in patients with Facioscapulohumeral muscular dystrophy 1 and preserved ejection fraction – assessment by cardiovascular magnetic resonance

BACKGROUND: Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is an autosomal dominant and the third most common inherited muscle disease. Cardiac involvement is currently described in several muscular dystrophies (MD), but there are conflicting reports in FSHD1. Mostly, FSHD1 is recognized as M...

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Detalles Bibliográficos
Autores principales: Blaszczyk, Edyta, Grieben, Ulrike, von Knobelsdorff-Brenkenhoff, Florian, Kellman, Peter, Schmacht, Luisa, Funk, Stephanie, Spuler, Simone, Schulz-Menger, Jeanette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487526/
https://www.ncbi.nlm.nih.gov/pubmed/31030674
http://dx.doi.org/10.1186/s12968-019-0537-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487526/
https://www.ncbi.nlm.nih.gov/pubmed/31030674
http://dx.doi.org/10.1186/s12968-019-0537-4

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