Jervell and Lange-Nielsen Syndrome 2 (JLNS2)

Alias:
Jlns2
Cardioauditory Syndrome of Jervell and Lange-Nielsen
Congenital Deafness and Functional Heart Disease
Prolonged Qt Interval in Ekg and Sudden Death
Jervell and Lange-Nielsen Syndrome, Type 2
Jervell-Lange Nielsen Syndrome
Long Qt Interval-Deafness
Surdo-Cardiac Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Jervell and Lange-Nielsen Syndrome 2, also known as jlns2, is related to jervell and lange-nielsen syndrome 1 and long qt syndrome 1, and has symptoms including syncope An important gene associated with Jervell and Lange-Nielsen Syndrome 2 is KCNE1 (Potassium Voltage-Gated Channel Subfamily E Regulatory Subunit 1). The drugs Ibutilide and Progesterone have been mentioned in the context of this disorder. Affiliated tissues include heart and heart-ventricle, and related phenotypes are prolonged qt interval and congenital sensorineural hearing impairment
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
8
5

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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