TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test sale cost 4400 AED
SDHD Gene Mitochondrial Complex II Deficiency Genetic Test sale cost 4400 AED SDHD Gene Mitochondrial Complex II Deficiency Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
DYSF Gene Miyoshi Myopathy Genetic Test sale cost 4400 AED DYSF Gene Miyoshi Myopathy Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test Cost

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

-21%

The TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the TK2 gene, which are associated with mitochondrial DNA depletion syndrome (MDS). This condition is a rare, autosomal recessive disorder that leads to a significant reduction in mitochondrial DNA in affected tissues, primarily impacting muscular and neurological functions. Symptoms can vary but often include muscle weakness, motor delays, and respiratory issues.

The test, priced at 4400 AED, involves collecting a DNA sample from the patient, usually through a blood draw, and analyzing it for specific genetic mutations in the TK2 gene. The results can provide crucial information for the diagnosis, management, and treatment planning of the syndrome, allowing for a more targeted approach to care. DNA Labs UAE utilizes advanced genetic sequencing technologies to ensure accurate and reliable testing outcomes, supporting patients and healthcare providers in navigating the complexities of mitochondrial DNA depletion syndrome.

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
Guaranteed Safe Checkout

TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test

At DNA Labs UAE, we offer the TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test. This test is designed to examine the TK2 gene for mutations associated with mitochondrial DNA depletion syndrome. Mitochondrial DNA depletion syndrome is a rare genetic disorder characterized by a reduction in the amount of mitochondrial DNA (mtDNA) in cells. This can lead to impaired mitochondrial function, affecting various organs and tissues in the body.

Test Components

  • 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

Prior to undergoing the TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic 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 TK2 Gene Mitochondrial DNA depletion syndrome. This information helps in better understanding the genetic context and potential implications of the test results.

Test Details

The TK2 Gene Mitochondrial DNA Depletion Syndrome NGS Genetic Test utilizes Next-Generation Sequencing (NGS) technology to analyze the TK2 gene for any mutations or genetic variations associated with mitochondrial DNA depletion syndrome. This comprehensive test allows for the simultaneous analysis of multiple genes, providing a detailed examination of the genetic makeup.

To perform the test, a DNA sample is required. This can be collected through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to analyze the entire TK2 gene, looking for any mutations or genetic variations that may be present.

The results of the TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test can help healthcare professionals in confirming a diagnosis of TK2 gene mitochondrial DNA depletion syndrome. Additionally, the test provides valuable information about the specific genetic variant involved, aiding in treatment decisions and assessing the risk of passing on the condition to future generations.

It is important to note that this genetic test should be ordered by healthcare professionals with expertise in genetics or genetic counseling. The results should be interpreted by a qualified healthcare professional who can provide appropriate genetic counseling and guidance based on the individual’s specific situation.

Test Name TK2 Gene Mitochondrial DNA depletion syndrome 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 TK2 Gene Mitochondrial DNA depletion syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TK2 Gene Mitochondrial DNA depletion syndrome
Test Details

TK2 gene mitochondrial DNA depletion syndrome NGS genetic test is a genetic test that examines the TK2 gene for mutations associated with mitochondrial DNA depletion syndrome. Mitochondrial DNA depletion syndrome is a rare genetic disorder characterized by a reduction in the amount of mitochondrial DNA (mtDNA) in cells. This can lead to impaired mitochondrial function, affecting various organs and tissues in the body.

The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the TK2 gene, to identify any genetic variations or mutations that may be present. This test can help in confirming a diagnosis of TK2 gene mitochondrial DNA depletion syndrome and provide information about the specific genetic variant involved.

The test involves collecting a DNA sample, typically through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology to analyze the entire TK2 gene, looking for any mutations or genetic variations. The results of the test can help healthcare professionals in determining the cause of symptoms, guiding treatment decisions, and providing information about the risk of passing on the condition to future generations.

It is important to note that this genetic test is typically ordered by healthcare professionals with expertise in genetics or genetic counseling. The results of the test should be interpreted by a healthcare professional who can provide appropriate genetic counseling and guidance based on the individual’s specific situation.

SKU: TEST-1719 Category:

Related products