Novel SCN5A gene mutation in a patient affected by multifocal ectopic premature Purkinje-related contractions syndrome.
Nicoletta VentrellaLorenzo BianchiniStefania RivaFrancesca PizzamiglioMaria Antonietta DessanaiFabrizio TundoTommaso SattinFrancesca De LioSelene CellucciClaudio TondoPublished in: ESC heart failure (2024)
We report the case of a 36-year-old woman who presented to the emergency department complaining of palpitations and asthenia. Investigations showed frequent ventricular ectopy and severe left ventricular ejection fraction impairment. She was diagnosed with a peculiar condition defined multifocal ectopic premature Purkinje-related contractions syndrome, which in some cases can be associated with a dilated cardiomyopathy phenotype. Genetic testing showed a novel mutation in the SCN5A gene (c.673C > G). In the context of acute left ventricular dysfunction in a young patient, we discuss the clinical presentation of this rare condition and its clinical management, as well as its genetic substrate.
Keyphrases
- left ventricular
- ejection fraction
- aortic stenosis
- case report
- emergency department
- heart failure
- hypertrophic cardiomyopathy
- genome wide
- cardiac resynchronization therapy
- acute myocardial infarction
- mitral valve
- transcatheter aortic valve replacement
- drug induced
- liver failure
- left atrial
- early onset
- aortic valve
- respiratory failure
- gene expression
- dna methylation
- intensive care unit
- middle aged
- atrial fibrillation
- coronary artery disease
- acute coronary syndrome
- amino acid
- mechanical ventilation
- percutaneous coronary intervention