What people are affected by hypertrophic cardiomyopathy?

HCM. Hypertrophic cardiomyopathy doesn't occur in any particular frequency in one group of people over another. It is relatively uncommon, being seen in about 1 in 500 people in the general population. However, it occurs in a hereditary form more than 50% of the time and therefore relatives of people with this disease should be screened for it.
Hypertrophic . It is a genetic disease, if you have it in your parents/ family there's a higher chance .
Depends. If its severe it usually affects atheletes and active people pts can have an arrythmia leading to sudden death. It can cause pts to faint. Especially if dehydrated. Treatment with a beta blocker and maybe a defibrillator.

Related Questions

What is hypertrophic cardiomyopathy?

IT IS A DISEASE OF. Your heart musclein which a part of the heart muscle is thickened or hypertrophied without any obvious cause. It is better known for causing silent, sudden cardiac death in otherwise healthy young people and athletes. Younger people are likely to have a more severe form of hcm. It is frequently free of symptoms until sudden cardiac death, and for this reason some suggest screening these youngsters. Read more...
HCM. Hypertrophic cardiomyopathy is a condition in which the heart muscle becomes thick, and obstruction to outflow may occur. Arrhythmias may occur as well. It is commonly inherited, first degree relatives should be screened. Patients may have severe symptoms, or no symptoms at all. It is a common cause of death in young athletes who seemed completely healthy. Read more...

Is hypertrophic cardiomyopathy serious?

Yes. Among young individuals, it is one of the leading causes of sudden death. A complete assessment by a cardiologist familiar with the condition can identify and recommend treatemtnto reduce the risk of sudden death. Read more...

Hpw bad is hypertrophic cardiomyopathy?

Depends. There is a range of phenotypes and manifestations. Hypertrophic cardiomyopathies can range from mild to severe. Read more...

Tell me about hypertrophic cardiomyopathy?

HCM. Hypertrophic cardiomyopathy is a condition in which the heart muscle becomes thick, and obstruction to outflow may occur. Arrhythmias may occur as well. It is commonly inherited, first degree relatives should be screened. Patients may have severe symptoms, or no symptoms at all. It is a common cause of death in young athletes who seemed completely healthy. Read more...

How can you get hypertrophic cardiomyopathy?

Genetic defect. Hypertrophic cardiomyopathy is caused by a mutation in one of several genes that codes for cardiac contractile proteins (sarcomeric proteins.) typically, these are inherited in an autosomal dominant pattern. Spontaneous mutations do occur. Over 50% of people have an affected parent, but disease expression is variable. Read more...

Why is hypertrophic cardiomyopathy dangerous?

Risk of death. Hypertrophic cardiomyopathy is the leading cause of death among young athletes. Further, individuals with this condition are at risk for sudden death even if they do not participate in sports. Read more...
3 Reasons. 1) unfavorable geometry - the heart is shaped the way it is to get a job done. Distortion of that geometry creates less effective action and blood flow 2) risk of sudden death - hcm screws up the electrical arrangement of the heart and increases risk of sudden death 3) obstruction - the very mass of the heart itself gets in the way of blood flow and causes chest pain and passing out. Read more...

Can you describe hypertrophic cardiomyopathy?

HCM. Hcm is an abnormal thickening usually of the wall (septum) that divides the right and left ventricle. This thickening occurs in the absence of other diseases known to cause thickening of the heart muscle. It is relatively uncommon but occurs in a familial/hereditary form more than 50% of the time. Therefore, siblings and children of patients with hcm should be screened for it. Read more...
HCM. Hypertrophic cardiomyopathy is an excessive thickening of the heart muscle. Hcm can be obstructive or nonobstructive. It is a genetic disorder. Symptoms may be mild, moderate, or severe. Sudden death may occur without warning from an arrhythmia. It was previously known as idiopathic hypertrophic subaortic stenosis (ihss). Read more...