Results 1 to 10 of about 106 (72)
La cardiopathie ischémique est fréquemment rencontrée chez les personnes infectées par le VIH. Cependant, les complications thromboemboliques sont rares. Nous rapportons une observation d’un homme admis en hospitalisation pour cardiomyopathie ischémique
Eugene kabanda, et. al
doaj +3 more sources
Abstract Introduction Aorto‐left ventricular tunnel (ALVT) accounts for <0.1% of congenital heart defects. Evidence on the prognosis from a fetal perspective is limited. With this retrospective international case series, we provide information on the outcome of fetuses with ALVT.
Amber E. L. van Nisselrooij +11 more
wiley +1 more source
From Hip to Heart: A Comprehensive Evaluation of an Infiltrative CardiomyopathyNovel Teaching Points
Infiltrative cardiomyopathies are an increasingly recognized cause of heart failure warranting systematic evaluation. Given overlap of clinical and imaging findings among etiologies of infiltrative cardiomyopathies, comprehensive evaluation, including a ...
Manavotam Singh, MD +9 more
doaj +1 more source
Dysfonction cardiaque sévère au cours du sepsis : à propos d'un cas
Le sepsis est une réponse inflammatoire de l´organisme secondaire à une infection documentée ou fortement suspectée. Le choc septique en est l´expression la plus grave.
Farid Pingwindé Belem +4 more
doaj +1 more source
A Case of Dilated Cardiomyopathy Associated With Chronic Toluene ExposureNovel Teaching Points
A 56-year-old woman working in a factory for the past 34 years presented with dilated cardiomyopathy of unknown etiology. She was exposed daily to toluene at work, without adequate protective equipment.
Gabrielle Denault, MD +3 more
doaj +1 more source
Les déficits en carnitine palmitoyltransférase (CPT) sont des atteintes rares dues à un défaut d´oxydation des acides gras. Patient de 10 ans sans antécédant présenteune dyspnée aigue associée à une toux productive dans un contexte fébrile et d ...
Imane Fetoui +4 more
doaj +1 more source
Cardiomyopathie dilatée : un mode de révélation peu fréquent du phéochromocytome
Le phéochromocytome est une tumeur neuroendocrine rare, sécrétant en excès des catécholamines et développé au dépend des cellules chromaffines de la médullosurrénale.
Mbarek Elkaouri +2 more
doaj +1 more source
Hypertrophic cardiomyopathy (HCM) is the primary cause of sudden cardiac death in children and adolescents. Patients with HCM frequently have ventricular tachycardia and ventricular fibrillation, although complete atrioventricular block (CAVB) is very ...
Hideharu Oka, MD, PhD +8 more
doaj +1 more source
Thrombosis, especially venous thromboembolism, is a complication often associated with coronavirus disease 2019 (COVID-19). However, there have been relatively few reports of arterial thrombosis.
Shohei Imaeda, MD +8 more
doaj +1 more source
Arrhythmia Monitoring for Risk Stratification in Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiomyopathy, presenting significant clinical heterogeneity. Arrhythmia risk stratification and detection are critical components in the evaluation and management of all cases of HCM.
Darson Du, MD +6 more
doaj +1 more source

