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Jervell-Lange Nielsen Syndrome

A form of long QT syndrome that is associated with congenital deafness. It is characterized by abnormal cardioelectrophysiology involving the VOLTAGE-GATED POTASSIUM CHANNEL. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).

Year introduced: 2002

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Tree Number(s): C14.280.067.565.440, C14.280.123.625.440, C16.131.240.400.715.440

MeSH Unique ID: D029593

Entry Terms:

  • Jervell Lange Nielsen Syndrome
  • Syndrome, Jervell-Lange Nielsen
  • Cardioauditory Syndrome of Jervell and Lange-Nielsen
  • Cardioauditory Syndrome of Jervell and Lange Nielsen
  • Cardio-Auditory-Syncope Syndrome
  • Cardio Auditory Syncope Syndrome
  • Cardio-Auditory-Syncope Syndromes
  • Syndrome, Cardio-Auditory-Syncope
  • Syndromes, Cardio-Auditory-Syncope
  • Deafness, Congenital, and Functional Heart Disease
  • Prolonged QT Interval in EKG and Sudden Death
  • Jervell and Lange-Nielsen Syndrome
  • Jervell and Lange Nielsen Syndrome
  • Surdo-Cardiac Syndrome
  • Surdo Cardiac Syndrome
  • Surdo-Cardiac Syndromes
  • Syndrome, Surdo-Cardiac
  • Jervell And Lange-Nielsen Syndrome 1
  • Jervell And Lange Nielsen Syndrome 1

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