Andersen Cardiodysrhythmic Periodic Paralysis (LQT7)

Alias:
Andersen Syndrome
Andersen-Tawil Syndrome
Lqt7
Long Qt Syndrome 7
Long Qt Syndrome Type 7
Ats
Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type
Andersen Tawil Syndrome
Potassium-Sensitive Cardiodysrhythmic Type
Long Qt Syndrome-7
Lqts Type 7
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Andersen Cardiodysrhythmic Periodic Paralysis, also known as andersen syndrome, is related to thyrotoxic periodic paralysis and graves disease 1, and has symptoms including syncope An important gene associated with Andersen Cardiodysrhythmic Periodic Paralysis is KCNJ2 (Potassium Inwardly Rectifying Channel Subfamily J Member 2), and among its related pathways/superpathways are Transmission across Chemical Synapses and Cardiac conduction. The drugs Acetazolamide and Carbonic Anhydrase Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include heart and kidney, and related phenotypes are muscle weakness and periodic paralysis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
<1/1000000
27
239
109

Medical Symptom

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Gene & Mutation

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Disease Model

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References Literature

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