What does hypertrophic cardiomyopathy mean?
Definitions for hypertrophic cardiomyopathy
hy·per·trophic car·diomy·opa·thy
This dictionary definitions page includes all the possible meanings, example usage and translations of the word hypertrophic cardiomyopathy.
Princeton's WordNet
hypertrophic cardiomyopathynoun
a disorder in which the heart muscle is so strong that it does not relax enough to fill with the heart with blood and so has reduced pumping ability
Wikipedia
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy (HCM, or HOCM when obstructive) is a condition in which the heart becomes thickened without an obvious cause. The parts of the heart most commonly affected are the interventricular septum and the ventricles. This results in the heart being less able to pump blood effectively and also may cause electrical conduction problems.People who have HCM may have a range of symptoms. People may be asymptomatic, or may have fatigue, leg swelling, and shortness of breath. It may also result in chest pain or fainting. Symptoms may be worse when the person is dehydrated. Complications may include heart failure, an irregular heartbeat, and sudden cardiac death.HCM is most commonly inherited in an autosomal dominant pattern. It is often due to mutations in certain genes involved with making heart muscle proteins. Other inherited causes of left ventricular hypertrophy may include Fabry disease, Friedreich's ataxia, and certain medications such as tacrolimus. Other considerations for causes of enlarged heart are athlete's heart and hypertension (high blood pressure). Making the diagnosis of HCM often involves a family history or pedigree, an electrocardiogram, echocardiogram, and stress testing. Genetic testing may also be done. HCM can be distinguished from other inherited causes of cardiomyopathy by its autosomal dominant pattern, whereas Fabry disease is X-linked and Friedreich's Ataxia is inherited in an autosomal recessive pattern.Treatment may depend on symptoms and other risk factors. Medications may include the use of beta blockers, verapamil or disopyramide. An implantable cardiac defibrillator may be recommended in those with certain types of irregular heartbeat. Surgery, in the form of a septal myectomy or heart transplant, may be done in those who do not improve with other measures. With treatment, the risk of death from the disease is less than one percent per year.HCM affects up to one in 200 people. Rates in men and women are about equal. People of all ages may be affected. The first modern description of the disease was by Donald Teare in 1958.
ChatGPT
hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy is a medical condition characterized by the thickening of the heart muscle, typically one part more than the others. This thickening can make it harder for the heart to pump blood, leading to a variety of symptoms like chest pain, fainting, and dizziness. It's often inherited and can affect people of all ages, although it's usually diagnosed during adolescence or young adulthood. In severe cases, hypertrophic cardiomyopathy can lead to heart failure or sudden cardiac death.
Wikidata
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy is a primary disease of the myocardium in which a portion of the myocardium is hypertrophied without any obvious cause. It is perhaps best known as a leading cause of sudden cardiac death in young athletes. The occurrence of hypertrophic cardiomyopathy is a significant cause of sudden unexpected cardiac death in any age group and as a cause of disabling cardiac symptoms. Younger people are likely to have a more severe form of hypertrophic cardiomyopathy. HCM is frequently asymptomatic until sudden cardiac death, and for this reason some suggest routinely screening certain populations for this disease. A cardiomyopathy is a disease that affects the muscle of the heart. With HCM, the sarcomeres in the heart increase in size, which results in the thickening of the heart muscle. In addition, the normal alignment of muscle cells is disrupted, a phenomenon known as myocardial disarray. HCM also causes disruptions of the electrical functions of the heart. HCM is most commonly due to a mutation in one of 9 sarcomeric genes that results in a mutated protein in the sarcomere, the primary component of the myocyte.
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Numerology
Chaldean Numerology
The numerical value of hypertrophic cardiomyopathy in Chaldean Numerology is: 1
Pythagorean Numerology
The numerical value of hypertrophic cardiomyopathy in Pythagorean Numerology is: 1
Translations for hypertrophic cardiomyopathy
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"hypertrophic cardiomyopathy." Definitions.net. STANDS4 LLC, 2024. Web. 29 Apr. 2024. <https://www.definitions.net/definition/hypertrophic+cardiomyopathy>.
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