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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