2023
DOI: 10.5334/jbsr.3064
|View full text |Cite
|
Sign up to set email alerts
|

Cardiac MRI after Sudden Cardiac Arrest in a Young Woman Prompts Diagnosis of Familial Dilated Cardiomyopathy

Abstract: Teaching Point: Familial dilated cardiomyopathy (DCM) predisposes to malignant ventricular arrhythmias and sudden cardiac death, and magnetic resonance imaging (MRI) has important diagnostic value in demonstrating non-ischemic patterns of late gadolinium enhancement (LGE).

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
0
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 1 publication
0
0
0
Order By: Relevance
“…The prevalence of DCM is 1:250, of which 30-50% are familial cases [29] and approximately 40% of cases have an identifiable genetic cause [30], and DCM is responsible for 1-3% of SCD cases in athletes [9].…”
Section: Dilated Cardiomyopathy (Dcm)mentioning
confidence: 99%
“…The prevalence of DCM is 1:250, of which 30-50% are familial cases [29] and approximately 40% of cases have an identifiable genetic cause [30], and DCM is responsible for 1-3% of SCD cases in athletes [9].…”
Section: Dilated Cardiomyopathy (Dcm)mentioning
confidence: 99%