Depends.... Depends. If you have significant obstruction to blood flow from the heart you may be asked to exercise to moderate levels only. Depending on the thickness of the septum, degree of obstruction, arrhythmias and family history your cardiologist may recommend a defibrillator which generally precludes high intensity sports. It all depends on the degree of severity of the condition.
Local answer best. The best answer for this question would come from the physicians who have examined the kid and are aware of his strengths and limitations. If well controlled, a broad area of possibilities may be present.
Light to moderate. Pt's with hoc should avoid all strenuous activity and competitive sports. Light to moderate amounts of activity are usually acceptable. Depending of the degree of lvot obstruction and if there is associated arrhythmia, medical or surgical rx may be necessary. Please check with your physician as this can be very serious and a cause of sudden death.
Not too physical. Generally would not perform jobs that involve heavy physical activity.
Hypertrophic cardio. Need to know how severe the hcm is, and what the family history of sudden death is, if that history is present. The job possibilities and their requirements should be discussed with the teen's cardiologist as many jobs are possible depending on the state of the myocardium and the family history of sudden death.
Non strenuous. The details should be discussed with one's personal physician, but most jobs that do not require strenuous physical labor would probably be do able. (teaching, clerical, administrative, lab etc...).
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.
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.
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.
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.
Hypertrophic. It is a genetic disease, if you have it in your parents/ family there's a higher chance.
Not acquired. Hypertrophic cardiomyopathy is caused by mutations of the proteins that make up the contractile apparatus of the heart, in general. That means it is not something you "get." generally, if you have the genetic makeup to cause hypertrophic cardiomyopathy, you should have evidence (abnormal echocardiogram) by 43 years of age, so if you have a normal echocardiogram you aren't going to develop hcm.
See cardiologist. Interested to know why you have this particular concern…I assume there is a family history? In any event, a screening ECG will be helpful, as these are generally markedly abnormal in the setting of HCM. An echocardiogram (ultrasound of the heart) can also assess for hypertrophy, and there may be genetic testing available if another family member has been diagnosed and a gene identified.