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Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome

Yıl 2021, Cilt: 2 Sayı: 2, 35 - 36, 11.10.2021

Öz

Brugada syndrome (BS) is an autosomal-dominant inherited genetic disorder characterized by mutations in cardiac sodium-channel genes, characteristic changes in electrocardiography (ECG) and associated with increased risk of ventricular arrhythmia and sudden cardiac death. BS mostly affects Asian races and its prevalence varies in different societies. Although it is a rare disease, it should be considered in patients admitted to the emergency department (ED) with the complaint of syncope. In a study, it was revealed that the main complaint in 28% of patients with BS was syncope. Here, we present a 19-year-old male patient who admitted to ED with the complaint of syncope and was diagnosed with BS.

Destekleyen Kurum

yok

Kaynakça

  • 1. Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol 1992;20:1391-6.
  • 2. Brugada J, Brugada P. What to do in patients with no structural heart disease and sudden arrhythmic death? Am J Cardiol 1996;78:69-75.
  • 3. Alings M, Wilde A. "Brugada" syndrome: clinical data and suggested pathophysiological mechanism. Circulation 1999;99:666-73.
  • 4. Miyasaka Y, Tsuji H, Yamada K, Tokunaga S, Saito D, Imuro Y, et al. Prevalence and mortality of the Brugada-type electrocardiogram in one city in Japan. J Am Coll Cardiol 2001;38:771-4.
  • 5. Matsuo K, Akahoshi M, Nakashima E, Seto S, Yano K. Clinical characteristics of subjects with the Brugada-type electrocardiogram:. J Cardiovasc Electrophysiol 2004;15:653-7.
  • 6. Patel SS, Anees S, Ferrick KJ. Prevalence of a Brugada pattern electrocardiogram in an urban population in the United States. Pacing Clin Electrophysiol 2009;32:704-8.
  • 7. Sacher F, Arsac F, Wilton SB, Derval N, Denis A, de Guillebon M, et al. Syncope in Brugada syndrome patients: prevalence, characteristics, and outcome. Heart Rhythm 2012;9:1272-9.
  • 8. Benito B, Sarkozy A, Mont L, Henkens S, Berruezo A, Tamborero D, et al. Gender differen-ces in clinical manifestations of Brugada syndrome. J Am Coll Cardiol 2008;52:1567-73.
  • 9. Brugada J, Brugada R, Brugada P. Determinants of sudden cardiac death in individuals with the electrocardiographic pattern of Brugada syndrome and no previous cardiac arrest. Circu-lation 2003;108:3092-6.
  • 10. Rodríguez-Mañero M, Namdar M, Sarkozy A, Casado-Arroyo R, Ricciardi D, de Asmundis C, et al. Prevalence, clinical characteristics and management of atrial fibrillation in patients with Brugada syndrome. Am J Cardiol 2013;111:362-7.
  • 11. Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. Heart Rhythm 2013;10:1932-63.
Yıl 2021, Cilt: 2 Sayı: 2, 35 - 36, 11.10.2021

Öz

Kaynakça

  • 1. Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol 1992;20:1391-6.
  • 2. Brugada J, Brugada P. What to do in patients with no structural heart disease and sudden arrhythmic death? Am J Cardiol 1996;78:69-75.
  • 3. Alings M, Wilde A. "Brugada" syndrome: clinical data and suggested pathophysiological mechanism. Circulation 1999;99:666-73.
  • 4. Miyasaka Y, Tsuji H, Yamada K, Tokunaga S, Saito D, Imuro Y, et al. Prevalence and mortality of the Brugada-type electrocardiogram in one city in Japan. J Am Coll Cardiol 2001;38:771-4.
  • 5. Matsuo K, Akahoshi M, Nakashima E, Seto S, Yano K. Clinical characteristics of subjects with the Brugada-type electrocardiogram:. J Cardiovasc Electrophysiol 2004;15:653-7.
  • 6. Patel SS, Anees S, Ferrick KJ. Prevalence of a Brugada pattern electrocardiogram in an urban population in the United States. Pacing Clin Electrophysiol 2009;32:704-8.
  • 7. Sacher F, Arsac F, Wilton SB, Derval N, Denis A, de Guillebon M, et al. Syncope in Brugada syndrome patients: prevalence, characteristics, and outcome. Heart Rhythm 2012;9:1272-9.
  • 8. Benito B, Sarkozy A, Mont L, Henkens S, Berruezo A, Tamborero D, et al. Gender differen-ces in clinical manifestations of Brugada syndrome. J Am Coll Cardiol 2008;52:1567-73.
  • 9. Brugada J, Brugada R, Brugada P. Determinants of sudden cardiac death in individuals with the electrocardiographic pattern of Brugada syndrome and no previous cardiac arrest. Circu-lation 2003;108:3092-6.
  • 10. Rodríguez-Mañero M, Namdar M, Sarkozy A, Casado-Arroyo R, Ricciardi D, de Asmundis C, et al. Prevalence, clinical characteristics and management of atrial fibrillation in patients with Brugada syndrome. Am J Cardiol 2013;111:362-7.
  • 11. Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, et al. HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. Heart Rhythm 2013;10:1932-63.
Toplam 11 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Klinik Tıp Bilimleri
Bölüm Olgu Sunumu
Yazarlar

Sertaç Güler 0000-0002-6266-6145

Dilber Üçöz Kocaşaban 0000-0002-7473-1434

Yayımlanma Tarihi 11 Ekim 2021
Gönderilme Tarihi 16 Ocak 2021
Kabul Tarihi 30 Ocak 2021
Yayımlandığı Sayı Yıl 2021 Cilt: 2 Sayı: 2

Kaynak Göster

APA Güler, S., & Üçöz Kocaşaban, D. (2021). Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome. Aksaray Üniversitesi Tıp Bilimleri Dergisi, 2(2), 35-36.
AMA Güler S, Üçöz Kocaşaban D. Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome. asujms. Ekim 2021;2(2):35-36.
Chicago Güler, Sertaç, ve Dilber Üçöz Kocaşaban. “Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome”. Aksaray Üniversitesi Tıp Bilimleri Dergisi 2, sy. 2 (Ekim 2021): 35-36.
EndNote Güler S, Üçöz Kocaşaban D (01 Ekim 2021) Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome. Aksaray Üniversitesi Tıp Bilimleri Dergisi 2 2 35–36.
IEEE S. Güler ve D. Üçöz Kocaşaban, “Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome”, asujms, c. 2, sy. 2, ss. 35–36, 2021.
ISNAD Güler, Sertaç - Üçöz Kocaşaban, Dilber. “Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome”. Aksaray Üniversitesi Tıp Bilimleri Dergisi 2/2 (Ekim 2021), 35-36.
JAMA Güler S, Üçöz Kocaşaban D. Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome. asujms. 2021;2:35–36.
MLA Güler, Sertaç ve Dilber Üçöz Kocaşaban. “Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome”. Aksaray Üniversitesi Tıp Bilimleri Dergisi, c. 2, sy. 2, 2021, ss. 35-36.
Vancouver Güler S, Üçöz Kocaşaban D. Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome. asujms. 2021;2(2):35-6.