Description

• Title:
  Brugada syndrome is still a current clinical problem. What do we know today - a literature review
• Creator:
  Misiło, Adriana;
  Sosna, Monika;
  Mordoń, Krzysztof
• Description:
  Brugada syndrome (BrS) is a rare congenital arrhythmia syndrome. BrS is characterized by a tendency to syncope, ventricular arrhythmias and sudden cardiac death. These symptoms occur mainly at night and can occur spontaneously or as a result of provocation by, for example, fever, stress or medication. Based on the differences in electrocardiography, three types were distinguished. Genetic studies are being conducted, which have shown a significant defect of the SCN5A gene, which in turn leads to disturbances in the functioning of the sodium channel NaV1.5 has a negative impact on the course of depolarization of myocardial cells. Patients with symptoms of the disease are subjected to implantation of a cardioverter-defibrillator, which protects them against sudden death. Data was obtained from the PubMed and Google Scholar platforms.
• Object availability:
  free access
• Rights: https://creativecommons.org/licenses/by-nc-sa/4.0 ;
  Prawa autorskie (c) 2023 Adriana Misiło, Monika Sosna, Krzysztof Mordoń
• Date:
  2023.08.29
• Type:
  info:eu-repo/semantics/article;
  info:eu-repo/semantics/publishedVersion
• Language:
  English
• Source:
  Journal of Education, Health and Sport; Vol. 46 No. 1 (2023); 176-184;
  Journal of Education, Health and Sport; Tom 46 Nr 1 (2023); 176-184;
  2391-8306
• Format:
  application/pdf
• Publisher:
  Nicolaus Copernicus University, Toruń, Poland
• Relation: https://apcz.umk.pl/JEHS/article/view/45367/36360
• Subject:
  sudden cardiac death;
  Brugada syndrome;
  ventricular arrhythmia
• Identifier: https://apcz.umk.pl/JEHS/article/view/45367
• Data provider:
  Akademicka Platforma Czasopism
• Can I use it?:
  seek permission
• Type:
  text