Heart Hypertrophy

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Information for Authority record
Name (Hebrew)
לב גידול יתר
Name (Latin)
Heart Hypertrophy
Other forms of name
Cardiac hypertrophy
Cardiomegaly
Enlargement of the heart
Heart
nne Heart
Heart enlargement
Hypertrophic cardiomyopathy
Myocardial hypertrophy
See Also From tracing topical name
Heart Diseases
Heart Size
MARC
MARC
Other Identifiers
Wikidata: Q1364270
Library of congress: sh 85059682
Sources of Information
  • LC data base, 1/31/91(Myocardial hypertophy)
  • Merck Manual(Hypertrophic myocardial disease)
  • MESH(Heart hypertrophy x Cardiac hypertrophy)
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Wikipedia description:

Hypertrophic cardiomyopathy (HCM, or HOCM when obstructive) is a condition in which muscle tissues of the heart become 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. Specifically, within the bundle branches that conduct impulses through the interventricular septum and into the Purkinje fibers, as these are responsible for the depolarization of contractile cells of both ventricles. 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 500 people. People of all ages may be affected. The first modern description of the disease was by Donald Teare in 1958. With a common occurrence amongst athletes there have been many cases among professional athletes. Danny Jones (rugby league) passed away during a rugby league game for Keighley Cougars against London Skolars in 2015 at the age of 29 . Footballer Fabrice Muamba survived a nearly fatal cardiac arrest during a game for Tottenham Hotspur in 2012. Muamba was saved by life saving treatment from medical staff at the game and a consultant cardiologist who was attending the game as a fan and entered the pitch once he saw what happening to Muamba.

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