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

Cilt: 2 Sayı: 2 11 Ekim 2021
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Senkopta Nadir Tanı: Tip 2 Brugada Sendromu / A Rare Diagnosis of Syncope: Type 2 Brugada Syndrome

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.

Anahtar Kelimeler

Destekleyen Kurum

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Kaynakça

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Ayrıntılar

Birincil Dil

İngilizce

Konular

Klinik Tıp Bilimleri

Bölüm

Olgu Sunumu

Yayımlanma Tarihi

11 Ekim 2021

Gönderilme Tarihi

16 Ocak 2021

Kabul Tarihi

30 Ocak 2021

Yayımlandığı Sayı

Yıl 2021 Cilt: 2 Sayı: 2

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