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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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[Apical hypertrophic cardiomyopathy--clinical and diagnostic characteristics based on a case report]

J Auer1, R Berent, H Mayr

  • 1II. Internen Abteilung mit Kardiologie des A. ö. Krankenhauses der Barmherzigen Schwestern vom Hl. Kreuz, Wels. johann.auer@khwels.at

Acta Medica Austriaca
|July 18, 2000
PubMed

Insights

Diagnosing hypertrophic non obstructive cardiomyopathy (HCM) can be challenging. This case report details a 77-year-old woman with long-standing chest pain, ultimately diagnosed with apical HCM via cardiac catheterization.

Area of Science:

  • Cardiology
  • Internal Medicine

Background:

  • Chest pain and shortness of breath are common symptoms.
  • Hypertrophic non obstructive cardiomyopathy (HCM) diagnosis can be difficult.
  • Differentiating HCM from coronary or hypertensive heart disease is crucial.

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