Spinocerebellar Ataxia Panel (SCA 1, 2, 3, 6, 7, 12, 17) in Colaba

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Sample Type

Blood

Recommended for

Male, Female

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WIthin 15 Days

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Overview

The Spinocerebellar Ataxia (SCA) Panel is a genetic test used to screen for specific types of spinocerebellar ataxias (SCAs). These are neurodegenerative disorders affecting balance, coordination, and movement. The panel analyzes mutations in genes associated with SCA 1, 2, 3, 6, 7, 12, and 17.

Genetic markers in autosomal dominant ataxias provide crucial insights into hereditary factors influencing the development of these disorders. Identifying specific markers aids in diagnosis, understanding inheritance patterns, and advancing research for effective therapeutic interventions. Early diagnosis can be crucial for managing symptoms and planning treatment options.

Spinocerebellar Ataxia Panel (SCA 1, 2, 3, 6, 7, 12, 17) Price in Colaba

Metropolis Healthcare is a leading diagnostics centre and pathology lab in India equipped with the latest state-of-the-art technologies that provides the Spinocerebellar Ataxia Panel (SCA 1, 2, 3, 6, 7, 12, 17) with a clear pricing structure

The price of Spinocerebellar Ataxia Panel (SCA 1, 2, 3, 6, 7, 12, 17) in Colaba is ₹ 16,000

We are committed to deliver accurate and quality results from the best labs in India with complete transparency regarding test cost and turnaround time. No matter where you are, we strive to offer patients high-quality service that is affordable and accessible.

Frequently Asked Questions

Why take Spinocerebellar Ataxia Panel (SCA 1, 2, 3, 6, 7, 12, 17)?

Test helps in early diagnosis and classification of SCA. Disease is characterized by a progressive in-coordination of walking. In addition, they are often associated with poor coordination of hand movements, eye movements, and speech

Is this test for you?

Test is recommended for clinically suspected spinocerebellar ataxia patients.

More Info on Spinocerebellar Ataxia Panel (SCA 1, 2, 3, 6, 7, 12, 17)

Genetic testing should be 1st carried out in most common SCAs such as SCA1, 2, and 3 followed by other subtypes if the first series test is negative. Recognition of a specific mutated gene helps to test the same gene in other family members.

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Why Metropolis?

Metropolis has a team of 200 senior pathologists and over 2000 technicians delivering diagnostic solutions in the areas of routine, semi specialty and super specialty domains like Oncology, Neurology, Gynaecology, Nephrology and many more.

We offer a comprehensive range of 4000+ clinical laboratory tests and profiles, which are used for prediction, early detection, diagnostic screening, confirmation and/or monitoring of the disease.