The long QT syndrome
Journal Title: Αρχεία Ελληνικής Ιατρικής - Year 2007, Vol 24, Issue 6
Abstract
The long QT syndrome is characterized by prolongation of the QT interval. Congenital syndromes related to QT prolongation and syncope or even sudden death were described many years ago. More recently six genetic loci for these congenital forms have been identified. Mutations in these genes prolong the action potential of isolated cells, resulting in the QT prolongation syndrome. Acquired causes of the long QT syndrome include drugs, electrolyte disorders and clinical syndromes due to other factors, such as HIV infection. The diagnosis of the long QT syndrome is based on clinical characteristics, electrocardiographic findings and family history. Short-term treatment aims at the prevention and correction of ventricular arrhythmias. Long-term treatment aims at shortening of the QT interval and the prevention of malignant arrhythmias.
Authors and Affiliations
M. PSALLAS, A. KOKKINOS, N. TENTOLOURIS
The mentally ill as a "spectacle" on the streets of Athens <br /> <br />
The history of psychiatry, as well as its achievements and progress, includes also some dark pages, when the mentally ill were demonstrated as a spectacle in the hospitals and the outpatient departments, and those wander...
The bio-medical comments of Empedocles. A precursor to modern science
Empedocles (Diogenis Laertius) was born in 490 ΒC, and lived in Akragas (Agrigento), Sicily. He died in 440 BC and was considered a physician and a philosopher. About 450 verses have been saved from his work, some of whi...
Determination of sibship by DNA analysis in Greeks
OBJECTIVE In cases where there is no parental DNA sample, a sibship determination is possible via specific DNA analysis. The aim of this study was to validate the efficiency of kinship analysis in the Greek population us...
Ameloblastoma (conventional, solid type)
No abstract available
The answer of listeners: Discussion with the audience
No abstract available