Jervell-Lange Nielsen Syndrome [Jervellův-Lange-Nielsenův syndrom]

topical
2
Terms

Jervellův a Langeho-Nielsenův syndrom
Jervellův-Lange-Nielsenův syndrom 1

 

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

Persistent link   https://www.medvik.cz/link/D029593
Definition

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).

DUI
D029593 MeSH Browser
CUI
M0012683
Previous indexing
Deafness (1969-1985); Long QT Syndrome (1986-2001)
History note
2002; use LONG QT SYNDROME 1986-2001
Public note
2002; see LONG QT SYNDROME 1986-2001

C Diseases
C14.280 Heart Diseases 2 858
C14.280.067 Arrhythmias, Cardiac 2 776
C14.280.067.565 Long QT Syndrome 217
C14.280.067.565.070 Andersen Syndrome 2
C14.280.067.565.440 Jervell-Lange Nielsen Syndrome 2
C14.280.067.565.720 Romano-Ward Syndrome 8
C14.280.123.625 Long QT Syndrome 217
C14.280.123.625.070 Andersen Syndrome 2
C14.280.123.625.440 Jervell-Lange Nielsen Syndrome 2
C14.280.123.625.720 Romano-Ward Syndrome 8
C16.131.240.400 Heart Defects, Congenital 1 558
C16.131.240.400.715 Long QT Syndrome 217
C16.131.240.400.715.070 Andersen Syndrome 2
C16.131.240.400.715.440 Jervell-Lange Nielsen Syndrome 2
C16.131.240.400.715.720 Romano-Ward Syndrome 8