spinocerebellar ataxia type 29

Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type I (ADCA type I) characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.

Also known as: SCA29, congenital nonprogressive spinocerebellar ataxia, spinocerebellar ataxia 29, congenital nonprogressive, spinocerebellar ataxia type 29, ACV, cerebellar ataxia early-onset nonprogressive, spinocerebellar ataxia 29.

Category: General

Looking into spinocerebellar ataxia type 29? See the lab tests healthcare providers may use to investigate spinocerebellar ataxia type 29, and learn what each one measures.
Explore tests for spinocerebellar ataxia type 29
Symptoms

Symptoms associated with spinocerebellar ataxia type 29

The following symptoms have been associated with spinocerebellar ataxia type 29 in medical literature. Not everyone experiences the same symptoms.

Tests

Tests used to investigate spinocerebellar ataxia type 29

Healthcare providers may order these tests when evaluating spinocerebellar ataxia type 29. Test selection is a clinical decision made by a qualified professional.

CBC with Differential

Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Related conditions

Conditions with overlapping symptoms

These conditions share symptoms with spinocerebellar ataxia type 29, which is why a clinical evaluation is important.

FAQ

Frequently Asked Questions

What is spinocerebellar ataxia type 29?

spinocerebellar ataxia type 29 is a health condition described in medical literature. Spinocerebellar ataxia type 29 (SCA29) is a rare subtype of autosomal dominant cerebellar ataxia type I (ADCA type I) characterized by very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability.

What are the symptoms of spinocerebellar ataxia type 29?

spinocerebellar ataxia type 29 is associated with 12 symptoms in the medical literature we index, including Action tremor, Bilateral facial palsy, Dysphagia, Focal impaired awareness seizure, Head tremor, Intention tremor. Symptoms vary widely between individuals.

How is spinocerebellar ataxia type 29 diagnosed or investigated?

A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with spinocerebellar ataxia type 29 include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. This information is educational, not a diagnosis.

Is SymptomDatabase.com diagnosing me?

No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have spinocerebellar ataxia type 29, please discuss your symptoms with a qualified healthcare provider.

Educational content only: The information on Symptom Database.com is for educational purposes and is not medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider. Read our full disclaimer.