| dc.creator |
Orhan, Semiha |
|
| dc.creator |
Eroglu, Fusun |
|
| dc.creator |
KARABACAK, Mustafa |
|
| dc.creator |
YILDIRIM, Mustafa Kemal |
|
| dc.creator |
Ceylan, Berit Gokce |
|
| dc.creator |
KARABACAK, Pınar |
|
| dc.date |
2017-07-31T21:00:00Z |
|
| dc.date.accessioned |
2020-10-06T10:59:49Z |
|
| dc.date.available |
2020-10-06T10:59:49Z |
|
| dc.identifier |
a994dca1-3c4d-49d1-a016-ff2accb77bc8 |
|
| dc.identifier |
10.4274/tybdd.92408 |
|
| dc.identifier |
https://avesis.sdu.edu.tr/publication/details/a994dca1-3c4d-49d1-a016-ff2accb77bc8/oai |
|
| dc.identifier.uri |
http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/68778 |
|
| dc.description |
Brugada syndrome is an electrocardiography (ECG) abnormality with a high incidence of sudden death in patients. It is characterized by typical ECG abnormalities such as ST elevation in precordial leads. Brugada syndrome is due to a mutation in the cardiac sodium channel genes. This syndrome can lead to a dangerous rhythm disorders such as ventricular fibrillation. Herein we presented a case who did not have any cardiac disorder, however had ventricular tachycardia and type 1 Brugada ECG pattern seen with cardiac arrest. |
|
| dc.language |
tur |
|
| dc.rights |
info:eu-repo/semantics/closedAccess |
|
| dc.title |
A Rare Case: Brugada Syndrome |
|
| dc.type |
info:eu-repo/semantics/article |
|