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  2. Hypertrophic cardiomyopathy - Wikipedia

    en.wikipedia.org/wiki/Hypertrophic_cardiomyopathy

    Even though hypertrophic cardiomyopathy (HCM) may be present early in life and is most likely congenital, it is one of the most-uncommon cardiac malformations encountered in pediatric cardiology, largely because the presentation of symptoms is usually absent, incomplete, or delayed into adulthood.

  3. How Hypertrophic Cardiomyopathy Progresses in Adults - AOL

    www.aol.com/hypertrophic-cardiomyopathy...

    At the time of diagnosis, most people with hypertrophic cardiomyopathy will have no symptoms and no evidence of an obstruction. Apart from follow-up monitoring, most won’t require treatment.

  4. 8 Common Cardiovascular Diseases for Men & How to Prevent Them

    www.aol.com/8-common-cardiovascular-diseases-men...

    Hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy develops when the walls of your left ventricle become thicker than normal. ... Symptoms of cardiovascular disease can vary depending on the ...

  5. Cardiomegaly - Wikipedia

    en.wikipedia.org/wiki/Cardiomegaly

    Hypertrophic cardiomyopathy screening [10] [11] Cardiomegaly (sometimes megacardia or megalocardia ) is a medical condition in which the heart becomes enlarged. It is more commonly referred to simply as "having an enlarged heart ".

  6. Cardiomyopathy - Wikipedia

    en.wikipedia.org/wiki/Cardiomyopathy

    Cardiomyopathy is a group of primary diseases of the heart muscle. [1] Early on there may be few or no symptoms. [1] As the disease worsens, shortness of breath, feeling tired, and swelling of the legs may occur, due to the onset of heart failure. [1]

  7. Athletic heart syndrome - Wikipedia

    en.wikipedia.org/wiki/Athletic_heart_syndrome

    Athlete's heart is not the cause of sudden cardiac death during or shortly after a workout, which mainly occurs due to hypertrophic cardiomyopathy and arrhythmogenic cardiomyopathy (ARVC), two genetic disorders. Although a link between intensive exercise and exercise-induced arrhythmogenic right ventricular cardiomyopathy exists. [3] [6]

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