一名 27 岁患者晕厥的意外原因：病例报告

Health Sciences Pub Date : 2024-05-01 DOI:10.35988/sm-hs.2024.089

Gerda Mierkytė, Benas Kireilis, Olesia Ivanova, Diana Rinkūnienė

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引用次数: 0

摘要

长 QT 综合征（LQTS）是一种罕见的遗传性心脏病，其特征是心电图（ECG）上出现 QT 间期延长和 T 波异常。它通常伴有晕厥，但也可能因心源性猝死（TdP）而发生。我们报告了一例 27 岁女性患者的病例，该患者经基因证实患有 LQTS 2 型 KCNH2 基因突变。在停用抗精神病药物并服用ß-肾上腺受体阻滞剂后，晕厥发作没有再发生。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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UNEXPECTED CAUSE OF SYNCOPE IN A 27 YEAR OLD PATIENT: CASE REPORT

Long QT syndrome (LQTS) is a rare inherited cardiac condition characterized by QT prolongation and T-wave abnormalities on the electrocardiogram (ECG). It is commonly associated with syncope, however, sudden cardiac death can occur due to Torsades de Pointes (TdP). We report the case of a 27-year-old female patient with genetically confirmed LQTS type 2 KCNH2 gene mutation found, who experienced multiple syncopes since a young age. After antipsychotic drugs were removed and ß-adrenoblockers were prescribed, fainting episodes did not reoccur.

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Health Sciences

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