Dilated Cardiomyopathy Case Reports
Dilated cardiomyopathy (DCM) is a significant myocardial disorder characterized by left ventricular dilation and impaired systolic function, often leading to heart failure, arrhythmias, thromboembolic events, and sudden cardiac death. Case Reports and Case Series in Cardiology Journal welcomes the submission of dilated cardiomyopathy case reports and case series that present rare clinical scenarios, diagnostic challenges, imaging findings, genetic associations, and therapeutic outcomes.
This dedicated section focuses on clinically meaningful reports involving idiopathic, familial, viral, ischemic, and secondary dilated cardiomyopathy, offering valuable educational insights for cardiologists, physicians, and clinical researchers.
We invite manuscripts covering:
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Idiopathic dilated cardiomyopathy
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Familial and genetic DCM cases
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Viral myocarditis progressing to DCM
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Postpartum dilated cardiomyopathy
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Alcohol-induced cardiomyopathy
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Chemotherapy-related cardiomyopathy
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Pediatric dilated cardiomyopathy
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Arrhythmia-associated DCM
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Advanced heart failure due to DCM
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Echocardiography and cardiac MRI findings
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Device therapy (ICD, CRT) case reports
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Long-term outcome and follow-up case series
At Case Reports and Case Series in Cardiology Journal, we encourage authors to submit rare, educational, and clinically impactful DCM cases that improve diagnosis, treatment planning, and patient outcomes.
Why Publish With Us?
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Rapid peer-review process
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DOI allocation for every article
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International editorial support
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Global visibility
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Ideal platform for cardiomyopathy case reports
Manuscript Submission
Authors are requested to submit their manuscript by using Online Manuscript Submission Portal: https://www.casereportsincardiology.org/submit.html (or) also invited to submit through the Journal E-mail Id: editor@casereportsincardiology.org.
