Case report: A rare case of left ventricular noncompaction in two Chinese siblings with becker muscular dystrophy caused by deletion of exons 10 to 12 in the DMD gene

BACKGROUND: Becker muscular dystrophy (BMD) is an inherited X-linked recessive condition resulting from mutations of the DMD gene encoding dystrophin. Left ventricular noncompaction (LVNC) is a rare cardiomyopathy morphologically characterized by abnormal myocardial trabeculae and deep recesses in t...

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Detalles Bibliográficos
Autores principales: Li, Jingdong, Zhu, Wanyue, Su, Guanhua, Zhu, Feng, Shuai, Xinxin, Meng, Yidi, Zhang, Jiaming, Chen, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538561/
https://www.ncbi.nlm.nih.gov/pubmed/37781315
http://dx.doi.org/10.3389/fcvm.2023.1243825

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538561/
https://www.ncbi.nlm.nih.gov/pubmed/37781315
http://dx.doi.org/10.3389/fcvm.2023.1243825

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