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ATM Gene Ataxia-Telangiectasia Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The ATM Gene Ataxia-Telangiectasia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the ATM gene, which are responsible for Ataxia-Telangiectasia (A-T), a rare, neurodegenerative, inherited disease. This condition is characterized by progressive loss of muscle control, immune system problems, and a high risk of cancer. The test plays a crucial role in the early identification and management of the disease, enabling healthcare providers to devise appropriate treatment and intervention strategies to improve the quality of life for affected individuals. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately analyze and interpret the genetic information. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a critical step for families seeking to understand their genetic health and manage the implications of Ataxia-Telangiectasia.

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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ATM Gene Ataxia-telangiectasia Genetic Test

Cost: AED 4400.0

Symptoms, Diagnosis, and Test Details

The ATM gene is responsible for producing a protein that helps repair damaged DNA. Mutations in the ATM gene can lead to a rare genetic disorder called ataxia-telangiectasia (A-T), which affects the nervous system, immune system, and increases the risk of cancer.

NGS (next-generation sequencing) genetic testing can be used to analyze the DNA sequence of the ATM gene and identify any mutations or variations that may be present. This can help diagnose A-T and provide information about the likelihood of passing on the condition to future generations.

NGS genetic testing is a highly accurate and efficient method of analyzing large amounts of genetic data. It can be used to analyze multiple genes at once, making it useful for diagnosing complex genetic disorders like A-T. NGS genetic testing can also be used to identify genetic variants that may increase the risk of developing certain diseases, such as cancer.

Test Components

  • Price: AED 4400.0
  • 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

Clinical History of Patient who is going for ATM Gene Ataxia-telangiectasia NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with ATM Gene Ataxia-telangiectasia

Test Name ATM Gene Ataxia-telangiectasia Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ATM Gene Ataxia-telangiectasia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ATM Gene Ataxia-telangiectasia
Test Details

The ATM gene is responsible for producing a protein that helps repair damaged DNA. Mutations in the ATM gene can lead to a rare genetic disorder called ataxia-telangiectasia (A-T), which affects the nervous system, immune system, and increases the risk of cancer.

NGS (next-generation sequencing) genetic testing can be used to analyze the DNA sequence of the ATM gene and identify any mutations or variations that may be present. This can help diagnose A-T and provide information about the likelihood of passing on the condition to future generations.

NGS genetic testing is a highly accurate and efficient method of analyzing large amounts of genetic data. It can be used to analyze multiple genes at once, making it useful for diagnosing complex genetic disorders like A-T. NGS genetic testing can also be used to identify genetic variants that may increase the risk of developing certain diseases, such as cancer.