La dysplasie arythmogène du ventricule droit (DAVD) est une cardiomyopathie d’ origine inconnue. C’est une maladie grave à l’origine de 20 % des morts. Arrêt cardiocirculatoire chez une adolescente et dysplasie arythmogène du ventricule droitCardiac arrest from arrhythmogenic right ventricular dysplasia in an. IRM et dysplasie arythmogène du ventricule droit (DAVD): Évaluation rétrospective chez 50 patientsMRI and arrhythmogenic right ventricular dysplasia (ARVD).

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It is characterized histologically by fatty or fibro-fatty infiltration of the right ventricular myocardium. Diagnostic criteria have been proposed for diagnosing ARVD.

Imaging, especially MRI, plays an important role. MR imaging must be performed using cardiac gating, and should include both cine-MR sequences for evaluation of segmental and global right ventricular function or any morphological change of the right ventricular shape, dysplzsie anatomic sequences to detect fatty or fibro-fatty infiltration of the right ventricular myocardium. Heart, arrhythmiaHeart, cardiomyopathyHeart, MR.


Outline Masquer le plan. Top of the page – Article Outline. Right ventricular cardiomyopathy and sudden death in young people.

N Engl J Med ; Br Heart J ; Arrythmogenic right ventricular cardiomyopathy: Diagnosis of arrythmogenic right ventricular dysplasia: Signifiance of morphological abnormalities detected by MRI in patients undergoing successful ablation of right ventricular outflow tract tachycardia. Right dysp,asie outflow tract ventricular tachycardia: J Am Coll Cardiol ; MR features of arrythmogenic right ventricular dysplasia.

Arrythmogenic right ventricular disease: MR imaging VS Angiography.

MR imaging of arrithmogenic right ventricular cardiomyopathy: MR evaluation of arrythmogenic right ventricular cardiomyopathy in pediatric patients.