| Autor: |
Fazel Mojtaba, Hamidi Fatemeh, Afshari Elham |
| Jazyk: |
angličtina |
| Rok vydání: |
2020 |
| Předmět: |
|
| Zdroj: |
Journal of Cardiovascular Emergencies, Vol 6, Iss 1, Pp 17-19 (2020) |
| Druh dokumentu: |
article |
| ISSN: |
2457-5518 |
| DOI: |
10.2478/jce-2020-0001 |
| Popis: |
Introduction: Brugada syndrome represents the clinical manifestation of a rare disease with genetic etiology. The syndrome is characterized by ventricular dysrhythmias associated with syncope or sudden cardiac death in the lack of any structural cardiac disease. The diagnosis of Brugada syndrome is established if a type 1 electrocardiographic (ECG) pattern of ST-segment and QRS morphology is present, in association with certain clinical manifestations and/or familial history. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
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