Idiopathic dilated cardiomyopathy in children: Prognostic indicators

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Ari M. E., Yoldas T., Orun U. A., Karademir S.

TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY, vol.47, no.3, pp.207-215, 2019 (ESCI)

• Publication Type: Article / Article
• Volume: 47 Issue: 3
• Publication Date: 2019
• Doi Number: 10.5543/tkda.2018.72809
• Journal Name: TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY
• Journal Indexes: Emerging Sources Citation Index (ESCI), Scopus, TR DİZİN (ULAKBİM)
• Page Numbers: pp.207-215
• Ankara Yıldırım Beyazıt University Affiliated: No

Abstract

Objective: Dilated cardiomyopathy (DCM) is a disorder featuring left ventricular dysfunction, heart failure, and a poor prognosis. The etiology is still unclear, despite diagnostic and therapeutic developments. This study was an evaluation of factors affecting the life span of a group of idiopathic DCM patients.