Arrhythmogenic cardiomyopathy is caused primarily by mutations in genes encoding desmosome proteins. Ventricular arrhythmias are the cardinal and typically early manifestations, whereas myocardial fibroadiposis is the pathological hallmark. HomozygousDSP(desmoplakin) andJUP(junction protein plakoglobin) mutations are responsible for a subset of patients with arrhythmogenic cardiomyopathy who exhibit cardiac arrhythmias and dysfunction, palmoplanter keratosis, and hair abnormalities (cardiocutaneous syndromes).
Distinct Cellular Basis for Early Cardiac Arrhythmias, the Cardinal Manifestation of Arrhythmogenic Cardiomyopathy, and the Skin Phenotype of Cardiocutaneous Syndromes / Karmouch, Jennifer; Zhou, Qiong Q; Miyake, Christina Y; Lombardi, Raffaella; Kretzschmar, Kai; Bannier-Hélaouët, Marie; Clevers, Hans; Wehrens, Xander H T; Willerson, James T; Marian, Ali J. - In: CIRCULATION RESEARCH. - ISSN 0009-7330. - 121:12(2017), pp. 1346-1359. [10.1161/CIRCRESAHA.117.311876]
Distinct Cellular Basis for Early Cardiac Arrhythmias, the Cardinal Manifestation of Arrhythmogenic Cardiomyopathy, and the Skin Phenotype of Cardiocutaneous Syndromes
Lombardi, Raffaella;
2017
Abstract
Arrhythmogenic cardiomyopathy is caused primarily by mutations in genes encoding desmosome proteins. Ventricular arrhythmias are the cardinal and typically early manifestations, whereas myocardial fibroadiposis is the pathological hallmark. HomozygousDSP(desmoplakin) andJUP(junction protein plakoglobin) mutations are responsible for a subset of patients with arrhythmogenic cardiomyopathy who exhibit cardiac arrhythmias and dysfunction, palmoplanter keratosis, and hair abnormalities (cardiocutaneous syndromes).File | Dimensione | Formato | |
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