Related Experiment Video
Updated: Aug 29, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
A fatal case of idiopathic restrictive cardiomyopathy
Przemysław Palka1, Aleksandra Lange, Cameron Ward
1St Andrew's Heart Institute & Department of Echocardiography, Prince Charles Hospital, Brisbane, Queensland, Australia. ppalka@hotmail.com
Abstract:
We describe the clinical features of idiopathic restrictive cardiomyopathy in a female infant. A marked elevation of left ventricular end-diastolic pressure, and profoundly abnormal myocardial relaxation, were detected with the use of Doppler blood flow echocardiography, coupled with the relatively new technique of Doppler tissue echocardiography. There was no clinical evidence of ongoing heart failure, but she had signs of myocardial ischaemia, and unfortunately died suddenly at the age of 13 months.
More Related Videos
Related Concept Videos
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Myocarditis I: Introduction
Rheumatic Heart Disease I: Introduction

