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Ataxia Gene Panel Test

Original price was: 9,600 د.إ.Current price is: 7,200 د.إ.

-25%

The Ataxia Gene Panel Test, available at DNA Labs UAE for 7200 AED, is a comprehensive diagnostic tool designed to identify genetic mutations associated with various forms of ataxia. Ataxia, a neurological condition characterized by impaired balance, coordination, and speech, can be caused by mutations in multiple genes. This panel test examines a broad spectrum of genes simultaneously to pinpoint the specific genetic alterations responsible for the condition in an individual.

By leveraging advanced genetic sequencing technologies, the test offers a precise and efficient approach to diagnosing different types of hereditary ataxias. This is particularly valuable for individuals exhibiting ataxia symptoms, families with a history of the condition, or those seeking a definitive genetic explanation for neurological symptoms of unknown cause. The information obtained from the test can guide clinical management, inform prognosis, and assist in family planning decisions.

Conducted at DNA Labs UAE, a facility renowned for its state-of-the-art genetic testing services, clients are assured of accurate and reliable results. The cost of the test is set at 7200 AED, reflecting the comprehensive nature of the analysis and the sophisticated technology employed.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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Ataxia Gene Panel Test

Cost: AED 7200.0

Symptoms and Diagnosis

Ataxia is a neurological disorder that affects coordination and balance. Symptoms may include difficulty walking, problems with coordination, slurred speech, and involuntary eye movements. The Ataxia Gene Panel Test is a diagnostic tool that analyzes a specific set of genes associated with ataxia to identify potential genetic mutations or variants responsible for causing the condition in a patient.

Test Components

  • Sterile container
  • Sterile Normal Saline Container
  • EDTA Vacutainer (3 ml)

Sample Condition

The Ataxia Gene Panel Test can be performed using amniotic fluid, chorionic villi, or peripheral blood samples.

Report Delivery

Reports are typically delivered within 4-6 weeks.

Method

The Ataxia Gene Panel Test utilizes Next-Generation Sequencing (NGS) technology to analyze the specific set of genes associated with ataxia.

Test Type

The Ataxia Gene Panel Test falls under the category of Genetics testing.

Referring Doctor

The Ataxia Gene Panel Test can be requested by a General Physician.

Test Department

The Ataxia Gene Panel Test is conducted in the Genetics department of DNA Labs UAE.

Pre Test Information

A doctor’s prescription is required to undergo the Ataxia Gene Panel Test. However, it is not applicable for surgery and pregnancy cases or individuals planning to travel abroad.

Test Details

The Ataxia Gene Panel Test analyzes a specific set of genes associated with ataxia, such as ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, and others. By identifying potential genetic mutations or variants in these genes, the test can confirm a diagnosis, guide treatment decisions, and provide information about the risk of passing on the condition to future generations.

Test Name Ataxia Gene Panel Test
Components Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer(3 ml)
Price 7200.0 AED
Sample Condition Amniotic fluid\/ Chorionic villi\/ Peripheral blood
Report Delivery 4-6 weeks
Method NGS
Test type Genetics
Doctor General Physician
Test Department:
Pre Test Information Ataxia Gene Panel can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

The Ataxia Gene Panel is a diagnostic tool that analyzes a specific set of genes associated with ataxia, a neurological disorder that affects coordination and balance. The panel typically includes genes such as ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A, and others. By analyzing these genes, the panel can identify potential genetic mutations or variants that may be responsible for causing ataxia in a patient. This information can be used to confirm a diagnosis, inform treatment decisions, and provide insight into the risk of passing on the condition to future generations.