Hypertrophic cardiomyopathy: Contemporary evaluation and management

Suwen Kumar, Howard Song, Meghan Chirpich, Stephen Heitner

Research output: Contribution to journalArticlepeer-review

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 2017

Keywords

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

ASJC Scopus subject areas

  • Medicine(all)

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