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Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

From: Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality

Fig. 3

The characteristics of cardiovascular magnetic resonance. The CMR of II: 3. a–c shows the delayed enhancement scanning PSIR images of T1W, T1W-FS and Gd-DTPA on the body axis. These images indicate the thickening of the free wall of the right ventricle with fat signal (a T1W, red arrow, and high signal; b lipid pressure of T1W, blue arrow, and low signal). Gd-DTPA delayed enhancement scanning shows mild local enhancement, suggesting the change of myocardial fibrosis. The CMR of II: 5. d–f shows the delayed enhancement scanning PSIR images of T1W, T1W-FS and Gd-DTPA on the body axis. These images indicate the thickening of the free wall of the right ventricle with fat signal (a T1W, red arrow, and high signal; b lipid pressure of T1W, blue arrow, and low signal). Figure g–i are the diastolic images of B-TFE film sequence for four-chamber heart, short-axis position and two-chamber heart of right ventricle, showing the obvious expansion of right atrium and right ventricular cavity

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172