Periodic Paralysis

Alias:
Familial Recurrent Paralysis
Familial Periodic Paralysis
Myotonic Periodic Paralysis
Myoplegic Dystrophy
Familial Myoplegia
Familial Paralysis
Periodic Myotonia
Westphal Disease
Cavarre Disease
Cavare Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Periodic Paralysis, also known as familial recurrent paralysis, is related to thyrotoxic periodic paralysis and hypokalemic periodic paralysis, type 1. An important gene associated with Periodic Paralysis is TBC1D24 (TBC1 Domain Family Member 24), and among its related pathways/superpathways are Cardiac conduction and Dopamine-DARPP32 Feedback onto cAMP Pathway. The drugs Lamotrigine and Diclofenamide have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and thyroid, and related phenotype is respiratory system.
Related ID:
ICD11:577112387

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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5
36
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Medical Symptom

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Description
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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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