Spinocerebellar Ataxia 4 (SCA4)

Alias:
Spinocerebellar Ataxia Type 4
Sca4
Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
Spinocerebellar Ataxia-4
Spinocerebellar Ataxias
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spinocerebellar Ataxia 4, also known as spinocerebellar ataxia type 4, is related to spinocerebellar ataxia, autosomal recessive 4 and spinocerebellar ataxia 13. An important gene associated with Spinocerebellar Ataxia 4 is PLEKHG4 (Pleckstrin Homology And RhoGEF Domain Containing G4). The drugs TA 0910 and Nootropic Agents have been mentioned in the context of this disorder. Affiliated tissues include cerebellum and cortex, and related phenotypes are impaired vibratory sensation and impaired proprioception
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
6
35
3

Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
Related Gene
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Publications
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References Literature

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