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What is Spinocerebellar ataxia 27?

What is Spinocerebellar ataxia 27?

  • Spinocerebellar ataxia 27: A rare genetic disorder (chromosome FGF14; 13q34 defect) characterized by tremors, dyskinesia and psychiatric episodes. Gait ataxia and dysarthria (speech disorder) also occur and are symptoms common to all the spinocerebellar ataxia types.

Spinocerebellar ataxia 27: Introduction

Types of Spinocerebellar ataxia 27:

Broader types of Spinocerebellar ataxia 27:

How serious is Spinocerebellar ataxia 27?

Prognosis of Spinocerebellar ataxia 27: normal life expectancy with major walking problems by 7th or 8th decade

What causes Spinocerebellar ataxia 27?

Causes of Spinocerebellar ataxia 27: see causes of Spinocerebellar ataxia 27

What are the symptoms of Spinocerebellar ataxia 27?

Symptoms of Spinocerebellar ataxia 27: see symptoms of Spinocerebellar ataxia 27

Onset of Spinocerebellar ataxia 27: childhood

Spinocerebellar ataxia 27: Testing

Diagnostic testing: see tests for Spinocerebellar ataxia 27.

Misdiagnosis: see misdiagnosis and Spinocerebellar ataxia 27.

How is it treated?

Doctors and Medical Specialists for Spinocerebellar ataxia 27: Medical Geneticist, Neurologist ; see also doctors and medical specialists for Spinocerebellar ataxia 27.
Treatments for Spinocerebellar ataxia 27: see treatments for Spinocerebellar ataxia 27

Name and Aliases of Spinocerebellar ataxia 27

Main name of condition: Spinocerebellar ataxia 27

Other names or spellings for Spinocerebellar ataxia 27:

SCA 27, spinocerebellar ataxia with tremor and dyskinesia, Cerebellar ataxia, autosomal dominant, FGF14-related

Spinocerebellar ataxia 27: Related Conditions

Research the causes of these diseases that are similar to, or related to, Spinocerebellar ataxia 27:

 

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