Hypertrophic Cardiomyopathy
Alternate Names : Asymmetric Septal Hypertrophy (ASH), Cardiomyopathy - Hypertrophic (HCM), Idiopathic Hypertrophic Subaortic Stenosis, IHSS
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Prognosis (Expectations)
Some affected individuals remain without symptoms for many years and have a normal life span, yet some may deteriorate gradually or rapidly. Progression into dilated cardiomyopathy occurs in some patients.
Patients with hypertrophic cardiomyopathy are at higher risk for sudden death than the normal population, and can be affected at a young age. Hypertrophic cardiomyopathy is a well known cause of sudden death in athletes. People with HCM should follow their doctor's advice about physical exercise and medical appointments.
Young patients with HCM planning to start a family may benefit from genetic counseling.
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