Novel Mutation of Plakophilin-2 Associated With Arrhythmogenic Right Ventricular Cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a disease characterized by dilatation and akinesis of the right ventricle, and causes life-threatening ventricular arrhythmia. Mutations of plakophilin-2 (PKP2) have recently been identified as one causative abnormality in ARVC. A case of ARV...

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Veröffentlicht in:Circulation Journal 2006, Vol.70(7), pp.933-935
Hauptverfasser: Nagaoka, Iori, Matsui, Keiji, Ueyama, Takeshi, Kanemoto, Masashi, Wu, Jie, Shimizu, Akihiko, Matsuzaki, Masunori, Horie, Minoru
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Sprache:eng
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Zusammenfassung:Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a disease characterized by dilatation and akinesis of the right ventricle, and causes life-threatening ventricular arrhythmia. Mutations of plakophilin-2 (PKP2) have recently been identified as one causative abnormality in ARVC. A case of ARVC with a mutation of PKP2 is reported here. Direct sequencing of the patient's DNA revealed an insertion mutation in exon 8 of PKP2 (1728_1729insGATG). The mutation caused the frameshift and the premature termination of translation (R577DfsX5). This is the first case report of PKP2 mutation found in Japanese ARVC patients. (Circ J 2006; 70: 933 - 935)
ISSN:1346-9843
1347-4820
DOI:10.1253/circj.70.933