We only find what we look for: fetal heart rate and the diagnosis of long-QT syndrome

Circ Arrhythm Electrophysiol. 2015 Aug;8(4):760-2. doi: 10.1161/CIRCEP.115.003196.

Abstract

Long QT syndrome (LQTS), an inherited channelopathy, is a common cause of arrhythmic death in infants, children and young adults. Although many LQTS genes have been identified, most (~75%) of LQTS mutations are found in KCNQ1, KCNH2 or SCN5A. In most cases, treatment for LQTS is successful and modifies the risk of life-threatening arrhythmias; thus, making the correct diagnosis is important. The diagnosis of LQTS is made by the measurement of a prolonged QT interval on the standard ECG; family history or characteristic arrhythmia features are used to strengthen the diagnosis and genetic testing confirms the diagnosis.

Keywords: Editorials; bradycardia; fetal; fetus; heart rate; infant; long QT syndrome.

Publication types

  • Editorial
  • Research Support, N.I.H., Extramural
  • Comment

MeSH terms

  • DNA / genetics*
  • Female
  • Fetal Diseases / genetics*
  • Heart Rate, Fetal / genetics*
  • Humans
  • KCNQ1 Potassium Channel / genetics*
  • Male
  • Mutation*
  • Pregnancy
  • Pregnancy Trimester, Third*
  • Romano-Ward Syndrome / genetics*

Substances

  • KCNQ1 Potassium Channel
  • DNA