9 Bilder zum Thema "long qt syndrome" bei ClipDealer

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A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.
3D illustration of an electrocardiogram (ECG) showing prolonged QT interval with broad-based T-waves, characteristic of type 1 long QT syndrome.
Male, 75 years old, clinically diagnosed as acute anterior septal and high lateral myocardial infarction.The culprit vessel was located in the LAD proximal segment.Prolonged QT interval with TDP.
Ventricular tachyarrhythmia includes many clinical types, some benign and some malignant. For malignant ventricular arrhythmias, patients are at risk of death.
Early afterdepolarization is an arrhythmogenic mechanism that triggers activity, occurring before the end of the T wave and commonly seen in QT interval prolongation.
A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.
Torsade de pointes refers to the pleomorphic ventricular tachycardia that occurs in the background of long QT interval, and the polarity of QRS wave twists around the equipotential line.
A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.
A 4-year-old boy with a clinical diagnosis of long QT syndrome. No genetic testing was done during hospitalization. The child died suddenly during follow-up.

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