The life expectancy of apical hypertrophic cardiomyopathy varies from a few months to a hundred or ten years, as sudden death is possible, but it is a minority, and most people do not die suddenly, and their life expectancy does not differ much from that of normal people. Apical hypertrophic cardiomyopathy is mostly non-obstructive cardiomyopathy, and its sudden death rate is significantly lower than that of obstructive cardiomyopathy. Patients with this type of cardiomyopathy are less likely to die suddenly, but they may have clinical manifestations, such as tightness in the chest, chest pain, dyspnea on exertion, dizziness, and fatigue, etc., although the symptoms can be controlled by medication.