ORTHOTOPIC CARDIAC TRANSPLANTATION IN A PATIENT WITH FAMILIAL RESTRICTIVE CARDIOMYOPATHY: CASE REPORT

Ercan Eren; Mustafa Güler; Suat Nail Ömeroğlu; Deniz Göksedef; Mete Alp; Cevat Yakut

Ercan Eren¹, Mustafa Güler¹, Suat Nail Ömeroğlu¹, Deniz Göksedef¹, Mete Alp¹, Cevat Yakut¹

¹Koşuyolu Kalp Eğitim ve Araştırma Hastanesi, Kalp Damar Cerrahisi Kliniği, İstanbul

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Restrictive cardiomyopathy is a rare disease which has a poor prognosis if it is left untreated. Etiologically, it may result from secondary to some storage diseases and/or primary (idiopathic) or familial. The definitive treatment is heart transplantation. We herein report a case with familial restrictive cardiomyopathy which has been the only one case in our heart transplantation series with 27 cases since 1989. Its diagnosis, follow-up, familial screening, and its treatment by a successful orthotopic heart transplantation with literature reviews are presented.

Keywords : Cardiomyopathy, restrictive, heart transplantation, familial

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