Prolonged QT interval in Rett syndrome

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Prolonged QT interval in Rett syndrome.

Rett syndrome is a severe neurodevelopmental disorder of unknown aetiology. A prolonged QT interval has been described previously in patients with Rett syndrome. To investigate QT prolongation and the presence of cardiac tachyarrhythmias in Rett syndrome electrocardiography and 24 hour Holter monitoring were performed prospectively in a cohort of 34 girls with Rett syndrome. The corrected QT va...

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Prolonged QT interval in the infants of diabetic mothers

Background: The prevalence of gestational diabetes mellitus is rising. Myocardial hypertrophy is the most common cardiac disorder in the infants of diabetic mothers, which hypothetically can cause fatal arrhythmias. This study investigated prolonged QT in the newborns of diabetic mothers in Afzalipour Hospital in Kerman City, in 2015. Methods: This case-contro...

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Beyond a prolonged QT interval

A 14-year-old girl was admitted with generalized tonic-clonic convulsions for 2min along with tongue biting. Her family reported previous recurrent attacks of muscle cramps and carpo-pedal spasms of four months’ duration prior to admission but they had never previously sought medical help. The patient had a good appetite and no diarrhea, with no prior history of cardiovascular disease or sympto...

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Prolonged QT interval: a tricky diagnosis?

Prolonged heart-rate adjusted QT intervals on the electrocardiogram (ECG) are associated with an increased risk for coronary heart disease and sudden death. However, the diagnosis of the prolonged QT interval is hampered by lack of standards. We studied variations in the prevalence of prolonged QT, based on different common definitions, in a large nonhospitalized population, and compared our re...

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[The long QT interval syndrome].

The syndrome of long QT interval frequently follows to syncope or a sudden cardiac death on the basis of originated polymorphic ventricular tachycardia of the "torsade de pointes" type. The prolongation of the QT interval in the hereditary form is based on mutation of the genes responsible for the formation of sodium and potassium channels. The authors analyze the occurrence, clinical findings,...

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ژورنال

عنوان ژورنال: Archives of Disease in Childhood

سال: 1999

ISSN: 0003-9888,1468-2044

DOI: 10.1136/adc.80.5.470