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Beyond Sarcomeric Hypertrophic Cardiomyopathy: How to Diagnose and Manage Phenocopies.

Maurizio PieroniMichele CiabattiElisa SalettiValentina TavantiPasquale SantangeliLucia MartineseFrancesco LiistroIacopo OlivottoLeonardo Bolognese
Published in: Current cardiology reports (2022)
In the last years, a wider application of genetic testing and the advances in cardiac imaging have significantly changed the diagnostic approach to HCM phenocopies. Different prognosis and management, with an increasing availability of disease-specific therapies, make differential diagnosis mandatory. The HCM phenotype can be the cardiac manifestation of different inherited and acquired disorders presenting different etiology, prognosis, and treatment. Differential diagnosis requires a cardiomyopathic mindset allowing to recognize red flags throughout the diagnostic work-up starting from clinical and family history and ending with advanced imaging and genetic testing. Different prognosis and management, with an increasing availability of disease-specific therapies make differential diagnosis mandatory.
Keyphrases
  • hypertrophic cardiomyopathy
  • left ventricular
  • high resolution
  • heart failure
  • combination therapy
  • fluorescence imaging
  • atrial fibrillation