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Jervell-Lange Nielsen Syndrome
(Jervell and Lange-Nielsen Syndrome)
Summary
Description:
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).
Also Known As:
Jervell and Lange-Nielsen Syndrome; Cardioauditory Syndrome of Jervell and Lange-Nielsen; Surdo-Cardiac Syndrome; Cardioauditory Syndrome of Jervell and Lange Nielsen; Jervell Lange Nielsen Syndrome Show All >>
Networked: 37
relevant articles (0 outcomes,
1 trials/studies)
for this Disease
Key Drugs and Agents for Jervell-Lange Nielsen Syndrome
Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
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Long QT syndrome type 1
:
1 study in 1 result
: IBA
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Potassium Channels (Potassium Channel)
:
5 results
: IBA
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Ion Channels (Ion Channel)
:
3 results
: IBA
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Iron
:
2 results
: IBA
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Gastrins
:
2 results
: IBA
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DNA (Deoxyribonucleic Acid)
:
2 results
: IBA
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Paroxysmal ventricular fibrillation
:
2 results
: IBA
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Timothy syndrome
:
2 results
: IBA
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Polymorphic catecholergic ventricular tachycardia
:
2 results
: IBA
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tranilast (N 5')
:
2 results
: IBA
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Diseases Related to Jervell-Lange Nielsen Syndrome
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Long QT Syndrome
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Romano-Ward Syndrome
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Deafness (Deaf Mutism)
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Cardiac Arrhythmias (Arrythmia)
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Arrhythmogenic Right Ventricular Dysplasia (Arrhythmogenic Right Ventricular Cardiomyopathy)
Show All >>
Key Therapies for Jervell-Lange Nielsen Syndrome
Efficacy Chart >>
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Cochlear Implantation
:
7 results
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Anesthesia
:
3 results
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Defibrillators (Defibrillator)
:
1 result
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Sympathectomy (Sympathectomies)
:
1 result
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Cochlear Implants (Cochlear Implant)
:
1 result
Show All >>
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