Electrocardiographic features of children with Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is a clinically common X-linked recessive myopathy, which is caused by mutation of the gene encoding dystrophin on chromosome Xp21. The onset of heart injury in children with DMD is inconspicuous, and the prognosis is poor once it develops to the stage of heart fail...

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Detalles Bibliográficos
Autores principales: Tang, Liting, Shao, Shuran, Wang, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392256/
https://www.ncbi.nlm.nih.gov/pubmed/35987773
http://dx.doi.org/10.1186/s13023-022-02473-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392256/
https://www.ncbi.nlm.nih.gov/pubmed/35987773
http://dx.doi.org/10.1186/s13023-022-02473-9

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