TY - JOUR
T1 - Hypertrophic cardiomyopathy
T2 - Contemporary evaluation and management
AU - Kumar, Suwen
AU - Song, Howard
AU - Chirpich, Meghan
AU - Heitner, Stephen
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017/3
Y1 - 2017/3
N2 - 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.
AB - 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.
KW - Hypertrophic cardiomyopathy
KW - Left ventricular outflow tract obstruction
KW - Sudden cardiac death
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M3 - Article
AN - SCOPUS:85026878422
SN - 0010-7069
VL - 57
JO - Consultant
JF - Consultant
IS - 3
ER -