Related Experiment Video

Updated: Jan 18, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Asymptomatic Apical Hypertrophic Cardiomyopathy Uncovered During Routine Preoperative Evaluation

Emily Strickland1, Takor B Arrey-Mbi2

  • 1Internal Medicine, Madigan Army Medical Center, Tacoma, USA.

Cureus
|September 8, 2025
PubMed

Insights

Apical hypertrophic cardiomyopathy (ApHCM) is a rare heart condition. Early EKG findings and advanced imaging confirmed ApHCM, prompting risk assessment for sudden cardiac death.

Area of Science:

  • Cardiology
  • Internal Medicine

Background:

  • Apical hypertrophic cardiomyopathy (ApHCM) is an uncommon, nonobstructive form of hypertrophic cardiomyopathy (HCM).
  • ApHCM is associated with increased risks of ventricular aneurysms, atrial fibrillation, heart failure, and cardiac death.

Keywords:
abnormal ekgapical hypertrophic cardiomyopathycardiac sudden deathekg abnormalitieshypertrophic cardiomyopathy (hcm)left ventricular hypertrophy (lvh)preoperative evaluationpreoperative planning

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