Hypertrophic cardiomyopathy: Contemporary evaluation and management

Suwen Kumar, Howard Song, Meghan Chirpich, Stephen Heitner

    Research output: Contribution to journalArticle

    Abstract

    Hypertrophic cardiomyopathy (HCM) is the most common monogenetic hereditary heart disease. With advances in cardiac imaging and genetics, an increasing number of patients with HCM are being identified. However, the condition remains underrecognized, largely because its clinical manifestations are unpredictable and vary among individuals even within the same family. The presentation ranges from sudden cardiac death to a completely benign course with no morbidity or impact on longevity. The overall prognosis of HCM is excellent, but it is this unpredictability that makes the diagnosis and management challenging, requiring a multifaceted approach.

    Original languageEnglish (US)
    JournalConsultant
    Volume57
    Issue number3
    StatePublished - Mar 1 2017

    Keywords

    • Hypertrophic cardiomyopathy
    • Left ventricular outflow tract obstruction
    • Sudden cardiac death

    ASJC Scopus subject areas

    • Medicine(all)

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  • Cite this

    Kumar, S., Song, H., Chirpich, M., & Heitner, S. (2017). Hypertrophic cardiomyopathy: Contemporary evaluation and management. Consultant, 57(3).