DISEASE SCANNER
Global Incurable Diseases Tracker
Hypertrophic Cardiomyopathy
A genetic condition causing abnormal thickening of the heart muscle, particularly the left ventricle. Most common cause of sudden cardiac death in young athletes. Can obstruct blood flow (obstructive HCM) or not (non-obstructive).
20.0M
89
Symptoms
Treatment Options
Risk Factors
Diagnostic Methods
- 1Echocardiogram
- 2Cardiac MRI
- 3Genetic testing
- 4ECG
- 5Holter monitor
- 6Exercise stress test
- 7Family screening
Prognosis
Generally good with modern care. Annual sudden death risk 1% (lower with ICD). Life expectancy near normal. Progressive heart failure in minority. Quality of life often excellent with treatment.
Prevention
- Genetic counseling
- Family screening
- Avoidance of competitive sports
- Adequate hydration
- Infection prevention (endocarditis)
- Regular cardiac follow-up
Research Status
Beta-blockers and calcium channel blockers first-line. Septal myectomy (surgical) for obstructive HCM. Alcohol septal ablation (minimally invasive). ICD for sudden death prevention. Genetic testing for family screening. Avoidance of competitive sports.
Affected Countries
Sources
- https://www.mayoclinic.org/diseases-conditions/hypertrophic-cardiomyopathy
- https://my.clevelandclinic.org/health/diseases/17679-hypertrophic-cardiomyopathy-hcm
- https://www.hematology.org/education/patients
- https://www.ncbi.nlm.nih.gov/books
- https://rarediseases.org/rare-diseases
Medical Disclaimer
This information is for educational purposes only. Always consult healthcare professionals for medical advice, diagnosis, and treatment.