Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report

Kiona Y. Allen*, Victoria L. Vetter, Maully J. Shah, Matthew J. O'Connor

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations
Original languageEnglish (US)
Pages (from-to)128-131
Number of pages4
JournalHeartRhythm Case Reports
Issue number2
StatePublished - Feb 1 2016


  • Dilated cardiomyopathy
  • Familial long QT syndrome
  • Genetics
  • KCNQ1
  • Voltage-gated potassium channel

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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