Fetal atrioventricular block and postpartum augmentative QT prolongation in a patient with long-QT syndrome with KCNQ1 mutation

J Cardiovasc Electrophysiol. 2010 Oct;21(10):1170-3. doi: 10.1111/j.1540-8167.2010.01758.x.

Abstract

The case of a 32-year-old pregnant woman, who had had several syncopal episodes during swimming and running at 9 and 10 years of age and whose fetus had 2:1 AV block, is presented. The mother and baby had the same heterozygous single nucleotide substitution in KCNQ1 at T587M. After 27 weeks of gestation, the fetal 2:1 AV block disappeared, and 1:1 AV conduction resumed, with a fetal heart rate of 110-120 beats/min. The maternal electrocardiogram revealed a normal QTc interval (433 ms) without ST-T abnormalities at gestational week 23, but the QTc was 490 and 531 ms at 1 and 2 months postpartum, with biphasic T waves in leads V2 and V3. This case is the first report of fetal 2:1 AV block with KCNQ1 mutation (T587M) and unmasked maternal QT prolongation in the postpartum period.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Atrioventricular Block / complications
  • Atrioventricular Block / diagnosis*
  • Atrioventricular Block / genetics*
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Heterozygote*
  • Humans
  • KCNQ Potassium Channels / genetics*
  • Long QT Syndrome / complications
  • Long QT Syndrome / diagnosis*
  • Long QT Syndrome / genetics*
  • Pregnancy

Substances

  • KCNQ Potassium Channels