Related Experiment Video
Updated: Dec 13, 2025

08:42
Cox-Maze IV Procedure Concomitant with Valvular Surgery In Situs Inversus Dextrocardia: A Single-Center Experience in China
Published on: February 11, 2022
4.0K
An ST-Elevation Myocardial Infarction In Situs Inversus Totalis (DEXTROCARDIA)
Granger Marsden1, Jessica Folk2, Jonathan Rosenberg3
1Department of Emergency Medicine, Cook County Health and Hospitals System, Chicago, Illinois.
The Journal of Emergency Medicine
|July 28, 2020
Abstract
No abstract available in PubMed .
More Related Videos
Related Concept Videos
Acute Coronary Syndrome I: Introduction
514
Acute Coronary Syndrome (ACS) encompasses a spectrum of heart conditions caused by sudden obstruction of coronary arteries, typically resulting from the rupture of an atherosclerotic plaque and subsequent thrombus (blood clot) formation. This obstruction can lead to partial or complete blockage of blood flow, causing varying degrees of myocardial ischemia or infarction.ACS includes the following clinical entities:Unstable Angina (UA)Non-ST-Elevation Myocardial Infarction (NSTEMI)ST-Elevation...
514
Mitral Stenosis II: Clinical features and Diagnostic Tests
126
Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
126
Cardiomyopathy III: Hypertrophic Cardiomyopathy
248
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
248

