Cardiomyopathy
- Introduction
- Dilated cardiomyopathy
- Hypertrophic cardiomyopathy
- Restrictive cardiomyopathy
Cardiomyopathy is a disease of the heart muscle.
It can be classified as primary or secondary and there are three main types of cardiomyopathy:
- Dilated
- Hypertrophic
- Restrictive
Hypertrophic cardiomyopathy involves abnormal growth or thickening of heart muscle (particularly the left ventricle). Due to thickening, the heart tends to stiffen and the size of the left ventricle may shrink, interfering with the heart's ability to deliver blood to all part of the body.
Causes
The cause of hypertrophic cardiomyopathy is not yet known. In the majority of cases the condition is inherited.
Symptoms
These include shortness of breath, chest pain, palpitation, light-headedness and blackouts. Can precipitate severe, even fatal tachyarrythmias.
In restrictive cardiomyopathy (RCM) the myocardium becomes rigid and less elastic, interfering with the expansion and filling of the ventricles with blood between contractions.
Causes
RCM can be idiopathic or secondary to cardiac and systemic disorders such as:
- Endomyocardial fibrosis
- Amyloidosis
- Sarcoidosis
- Gaucher's disease
- Mucopolysaccharidoses
- Carcinoid syndrome
Symptoms
These include fatigue, shortness of breath and oedema.