Long QT Syndrome: Difference between revisions

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The Long QT syndrome is characterized on the ECG by prolongation of the heart rate corrected QT interval [[Geleidingstijden_%28PQ%2CQRS%2CQT%29|QT tijd]]. It was first recognized by dr. Jervell and dr. Lange-Nielsen in 1957, accompanied by hearing deficits, sudden cardiac death and an autosomal recessive inheritance.<cite>Lang1957</cite>
The Long QT syndrome is characterized on the ECG by prolongation of the [[Conduction#The_QT_interval|heart rate corrected QT interval]]. It was first recognized by dr. Jervell and dr. Lange-Nielsen in 1957, accompanied by hearing deficits, sudden cardiac death and an autosomal recessive inheritance.<cite>Lang1957</cite>


The Long QT syndrome is characterized
The Long QT syndrome is characterized
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