Spinocerebellar Ataxia 20 (SCA20)

Alias:
Spinocerebellar Ataxia Type 20
Sca20
Spinocerebellar Ataxia with Spasmodic Cough
Spinocerebellar Ataxia with Dysphonia
Chromosome 11q12 Duplication Syndrome, 260-Kb
Chromosome 11q12 Duplication Syndrome 260-Kb
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spinocerebellar Ataxia 20, also known as spinocerebellar ataxia type 20, is related to aceruloplasminemia and autosomal dominant cerebellar ataxia, and has symptoms including myoclonus, palatal, action tremor and static tremor. An important gene associated with Spinocerebellar Ataxia 20 is SCA20 (Spinocerebellar Ataxia 20). Affiliated tissues include spinal cord and cerebellum, and related phenotypes are dysarthria and dysphonia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
<1/1000000
7
42
11

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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References Literature

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