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).
推出的年份: 2002
树号: C14.280.067.565.440, C14.280.123.625.440, C16.131.240.400.715.440
MeSH 单一 ID: D029593
进入的组:
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
早前的内容:
Deafness (1969-1985)
Long QT Syndrome (1986-2001)
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