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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A Case Report on the Atypical Presentation of Hypertrophic Cardiomyopathy (HOCM) in a 19-Year-Old Female

Ahmed Alhazmi1, Shahad B Almatrafi2, Rahaf A Abdulwahab3

  • 1Cardiology, King Abdullah Medical City, Makkah, SAU.

Cureus
|January 5, 2023
PubMed

Insights

Atypical hypertrophic cardiomyopathy (HOCM) can present as biventricular hypertrophy, even in asymptomatic patients without a family history. Early awareness is crucial for preventing sudden cardiac death (SCD) associated with this rare genetic disorder.

Area of Science:

  • Cardiology
  • Genetics
  • Internal Medicine

Background:

  • Atypical hypertrophic cardiomyopathy (HOCM) is a rare genetic disorder affecting the left ventricle.
  • HOCM is a known risk factor for sudden cardiac death (SCD).

Keywords:
cardiologycase reporthocmhypertrophic cardiomyopathysaudi arabia

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