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Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

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...
Layers of the Heart Wall01:15

Layers of the Heart Wall

The heart wall comprises three distinct layers: the epicardium, myocardium, and endocardium. The outermost layer, the epicardium, is the visceral layer of the serous pericardium, featuring a thin, transparent mesothelial surface and an inner layer of areolar connective tissue with fat deposits that increase with age.
The myocardium, the thickest layer, consists of cardiac muscle cells interconnected by intercalated discs and crisscrossing connective tissue fibers. These muscle fibers contract...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
Mitral Stenosis I: Introduction01:22

Mitral Stenosis I: Introduction

Mitral Valve Stenosis (MVS) is a heart condition where the mitral valve narrows, impeding blood circulation from the left atrium to the left ventricle. The etiology and pathophysiology of this condition are multifaceted, leading to a cascade of cardiovascular complications.Causes of Mitral Valve StenosisRheumatic Heart Disease: It is the main cause of mitral valve stenosis, particularly in developing nations. This condition arises from rheumatic fever, an inflammatory illness resulting from...

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Related Experiment Video

Updated: Jun 14, 2026

En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos
08:57

En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos

Published on: July 27, 2022

Partial Endocardial Cushion Defects.

C L Robinson, J E Merriman, C J Kilduff

    Canadian Medical Association Journal
    |March 24, 2010
    PubMed
    Summary
    This summary is machine-generated.

    Seven patients with endocardial cushion defects underwent surgical repair without mortality. Diagnosis utilized electrocardiography and cardiac catheterization, with left bundle branch aberration noted. Careful surgical technique is crucial to avoid bundle of His damage.

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    Isolation of Endocardial and Coronary Endothelial Cells from the Ventricular Free Wall of the Rat Heart
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    Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
    07:41

    Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure

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    Related Experiment Videos

    Last Updated: Jun 14, 2026

    En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos
    08:57

    En Face Endocardial Cushion Preparation for Planar Morphogenesis Analysis in Mouse Embryos

    Published on: July 27, 2022

    Isolation of Endocardial and Coronary Endothelial Cells from the Ventricular Free Wall of the Rat Heart
    08:22

    Isolation of Endocardial and Coronary Endothelial Cells from the Ventricular Free Wall of the Rat Heart

    Published on: April 15, 2020

    Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
    07:41

    Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure

    Published on: February 8, 2022

    Area of Science:

    • Cardiology
    • Congenital Heart Disease
    • Cardiac Surgery

    Background:

    • Endocardial cushion defects (ECDs) are a group of congenital heart abnormalities.
    • Surgical intervention is often necessary for significant ECDs.
    • Potential complications include damage to the cardiac conduction system.

    Purpose of the Study:

    • To report surgical outcomes for partial endocardial cushion defects.
    • To highlight diagnostic methods and characteristic findings.
    • To emphasize potential surgical complications.

    Main Methods:

    • Surgical repair of seven partial endocardial cushion defects.
    • Diagnostic evaluation included electrocardiography (ECG), vector-cardiography, radiography, and cardiac catheterization.
    • Analysis of ECG findings (left axis deviation, right ventricular hypertrophy) and vector-cardiographic patterns.

    Main Results:

    • Seven patients underwent surgical repair with zero mortality.
    • Six cases were ostium primum type, one involved a left ventricle to right atrium defect.
    • Diagnostic findings included specific ECG/vector-cardiographic patterns, cardiac enlargement, and oxygen saturation changes during catheterization.

    Conclusions:

    • Surgical repair of partial endocardial cushion defects can be performed with excellent outcomes.
    • Characteristic ECG and vector-cardiographic findings aid in diagnosis, often indicating left bundle branch aberration.
    • Minimizing damage to the bundle of His during surgery is a critical consideration.