(III-1A.5.o) 49-year old female with cardiac failure and mitochondrial myopathy M. Dzieciuch-Rojek, P. Rubiś MD, PhD, S. Wiśniowska-Śmiałek MD, J. Stępniewski MD, D. Kudliński MD, A. Leśniak-Sobelga MD, PhD, M. Kostkiewicz MD, PhD, Prof. P. Podolec MD, PhD

  BRIEF COMMENTS EXPERT: Assoc. Prof. Bogusław Kapelak MD, PhD Affiliation: Department of Cardiovascular Surgery and Transplantology, John Paul II Hospital, Krakow, Poland COMMENT There are indications for heart transplantation in this patient. A very important issue is the comprehensive assessment of the patient before surgery, in particular neurological evaluation for possible post-operative complications (if there is a risk of respiratory failure) and the ability of the patient to participate in post-transplant rehabilitation. EXPERT: Prof. Andrzej Rudziński MD, PhD Affiliation: …

Posted in 1. Dilated cardiomyopathy, 5. Medication-induced, A. Genetic, Case presentations, III. Rare diseases of the heart (cardiomyopathies) | Leave a comment

(III-1A.1) 24 years old male with ventricular arrhythmia and family history of dilated cardiomyopathy and sudden cardiac deaths. Jakub Stępniewski MD, Paweł Rubiś MD, PhD, Agata Leśniak-Sobelga MD PhD, Magdalena Kostkiewicz MD, PhD.

https://i1.wp.com/www.crcd.eu/wp-content/uploads/2013/07/schema11.png?fit=190%2C120

Background Dilated cardiomyopathy (DCM) is a clinical condition in which left ventricle (LV) dilation and subsequent impairment of its systolic function is caused by primary myocardial dysfunction [1]. The potential causes of LV dilation are vast and include myocardial destruction in the course of coronary heart diseases, toxic, infectious, or metabolic reasons [1 ESC]. Approximately 20-35% of cases with undetermined etiology are expected to have a familial form of DCM [2]. Familial DCM (FDCM) is in the vast majority a …

Posted in 1. Dilated cardiomyopathy, A. Genetic, Case presentations, III. Rare diseases of the heart (cardiomyopathies) | Leave a comment

(III-1B.1.o) 29-years old patient with heart and renal failure Anton Chrustowicz, Jolanta Rzucidło

Authors: Anton Chrustowicz 1 , Jolanta Rzucidło 1 1John Paul II Hospital in Krakow   case presentations and videos are provided for private use only

Posted in 1. Dilated cardiomyopathy, 1. Inflammatory cardiomyopathy, B. Nongenetic, Case presentations, III. Rare diseases of the heart (cardiomyopathies) | Leave a comment

(III-1A.4b) Dilated cardiomyopathy with atriovantricular conduction defects in patient Marchel M., Opolski G.

https://i1.wp.com/www.crcd.eu/wp-content/uploads/2011/09/CC_Paris_header.png?fit=190%2C23

  case presentations and videos are provided for private use only

Posted in 1. Dilated cardiomyopathy, 4. Nuclear membrane mutations, A. Genetic, Case presentations, III. Rare diseases of the heart (cardiomyopathies) | Leave a comment