Related Experiment Video
Updated: Jun 6, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Asymmetric septal hypertrophic cardiomyopathy: a case report
1Department of Radiology, Henry Ford Hospital, 2799 West Grand Blvd, Detroit, MI 48202, USA. matthewr@rad.hfh.edu
Abstract:
We report the case of a 30-year-old female who presented to the emergency department with the chief complaint of syncope. She also described intermittent chest pain and exertional dyspnea over the past several weeks. Review of systems and laboratory findings including D: -dimer levels were noncontributory. EKG demonstrated right bundle branch block. Nongated chest CT with contrast was ordered to exclude the possibility of pulmonary embolism demonstrating markedly asymmetric septal thickening. Suspicion for hypertrophic cardiomyopathy was raised, which was subsequently confirmed on gated cardiac MRI.
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Mitral Stenosis II: Clinical features and Diagnostic Tests