dysplasia

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Related to Arrhythmogenic right ventricular dysplasia: Arrhythmogenic right ventricular cardiomyopathy

dysplasia

[di′splā·zhə]
(pathology)
Abnormal development or growth, especially of cells.
References in periodicals archive ?
Evidence of apoptosis in arrhythmogenic right ventricular dysplasia.
Familial form of arrhythmogenic right ventricular dysplasia.
Arrhythmogenic right ventricular dysplasia presenting with ventricular tachycardia in a father and son.
The term arrhythmogenic right ventricular dysplasia was first used by Frank et al.
Role of cardiovascular magnetic resonance imaging in arrhythmogenic right ventricular dysplasia.
Cardiomyopathies such as hypertrophic cardiomyopathy, dilated cardiomyopathy and arrhythmogenic right ventricular dysplasia account for approximately 10-15 per cent of sudden deaths (2).
Other indications included aborted SCD, long QT syndrome with family history of SCD, hypertrophic obstructive cardiomyopathy with family history of SCD, arrhythmogenic right ventricular dysplasia, recurrent syncope, bradycardia, and refractory paroxysmal atrial flutter.

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