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Ataxia Comprehensive Panel NGS Genetic Test Cost

Original price was: 6,000 د.إ.Current price is: 4,400 د.إ.

-27%

The Ataxia Comprehensive Panel NGS Genetic Test is a cutting-edge diagnostic tool available at DNA Labs UAE, designed to identify genetic mutations associated with various forms of ataxia, a neurological disorder that affects coordination, balance, and speech. This test utilizes Next Generation Sequencing (NGS) technology, which allows for the simultaneous examination of multiple genes associated with ataxia, providing a comprehensive analysis of the patient’s genetic makeup.

At a cost of 4400 AED, the test is an investment in pinpointing the specific genetic alterations that may be responsible for ataxic symptoms, facilitating a more tailored approach to treatment and management of the condition. By identifying the genetic underpinnings of ataxia, healthcare providers can offer patients more personalized care plans, potentially improving outcomes and quality of life.

DNA Labs UAE, where this test is conducted, is equipped with state-of-the-art technology and staffed by experts in the field of genetic testing, ensuring that patients receive accurate and reliable results. This test represents an important step forward in the field of neurogenetics and offers hope to individuals and families affected by ataxia, providing them with critical information that can guide their healthcare decisions.

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Ataxia Comprehensive Panel NGS Genetic Test

Welcome to DNA Labs UAE, where we offer the Ataxia Comprehensive Panel NGS Genetic Test. This test is designed to analyze a panel of genes associated with different types of ataxia, which are neurological disorders characterized by movement and coordination problems.

Test Details

The Ataxia Comprehensive Panel NGS Genetic DNA Test is a genetic test that uses next-generation sequencing (NGS) technology to identify genetic mutations that may be responsible for the development of ataxia. The panel includes genes associated with spinocerebellar ataxia, Friedreich ataxia, episodic ataxia, and other types of ataxia.

Test Components

The Ataxia Comprehensive Panel NGS Genetic DNA Test includes a comprehensive analysis of the genes associated with ataxia.

  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the Ataxia Comprehensive Panel NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with ataxia comprehensive panel.

Diagnosis and Personalized Treatment

The Ataxia Comprehensive Panel NGS Genetic DNA Test can help diagnose ataxia and identify the underlying genetic cause of the condition. This information can aid in the development of personalized treatment and management strategies for individuals with ataxia.

 

Test NameAtaxia comprehensive panel NGS Genetic DNA Test
Components 
Price4400.0 AED
Sample ConditionBlood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery3 to 4 Weeks
MethodNGS Technology
Test typeNeurological Disorders
DoctorNeurologist
Test Department:Genetics
Pre Test InformationClinical History of Patient who is going for Ataxia comprehensive panel NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Ataxia comprehensive panel
Test DetailsThe Ataxia Comprehensive Panel NGS Genetic DNA Test is a genetic test that analyzes a panel of genes associated with different types of ataxia, a group of neurological disorders characterized by problems with movement and coordination. The test uses next-generation sequencing (NGS) technology to identify genetic mutations that may be responsible for the development of ataxia. The panel includes genes associated with spinocerebellar ataxia, Friedreich ataxia, episodic ataxia, and other types of ataxia. The test can help diagnose ataxia and identify the underlying genetic cause of the condition, which can aid in personalized treatment and management strategies.