TTPA Gene Vitamin E Familial Deficiency Genetic Test sale cost 4400 AED
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TTPA Gene Vitamin E Familial Deficiency Genetic Test Cost

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

-21%

The TTPA gene plays a crucial role in the human body by encoding the alpha-tocopherol transfer protein, which is essential for the proper distribution and regulation of vitamin E, a crucial antioxidant that protects cells from damage. Mutations in the TTPA gene can lead to a rare, autosomal recessive disorder known as Vitamin E deficiency or Ataxia with Vitamin E Deficiency (AVED), which can cause neurological problems, muscle weakness, and coordination issues.

To diagnose this genetic condition, a specific genetic test is available that examines the TTPA gene for mutations. This test is crucial for individuals who have symptoms of Vitamin E deficiency or have a family history of the condition, as early detection and treatment can significantly improve the quality of life and prevent the progression of symptoms.

In the UAE, this genetic test is offered by DNA Labs UAE, a reputable laboratory known for its advanced genetic testing services. The cost of the TTPA Gene Vitamin E Familial Deficiency Genetic Test is 4400 AED. This test is performed using a sample of the patient’s blood or saliva, and it involves analyzing the genetic material to identify any mutations in the TTPA gene. The results of this test can provide valuable information for the diagnosis and management of Vitamin E deficiency, allowing for personalized treatment plans that may include dietary adjustments and Vitamin E supplementation to mitigate the symptoms associated with the condition.

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TTPA Gene Vitamin E Familial Deficiency Genetic Test

At DNA Labs UAE, we offer the TTPA Gene Vitamin E familial deficiency Genetic Test to diagnose and manage individuals with suspected vitamin E familial deficiency. This comprehensive genetic test utilizes NGS (Next-Generation Sequencing) technology to analyze the TTPA gene and identify specific mutations responsible for this condition.

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 TTPA Gene Vitamin E familial deficiency Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with TTPA Gene Vitamin E familial deficiency. This information will aid in the accurate interpretation of the test results.

Test Details

The TTPA gene is responsible for producing a protein called alpha-tocopherol transfer protein (TTP), which plays a crucial role in the transport of vitamin E in the body. Mutations in the TTPA gene can result in a condition known as vitamin E familial deficiency.

Vitamin E familial deficiency is an autosomal recessive disorder characterized by a reduced ability to absorb and transport vitamin E in the body. This deficiency can lead to oxidative damage to cells, as vitamin E is an essential antioxidant that protects against such damage.

NGS genetic testing is a state-of-the-art technique that allows for the simultaneous analysis of multiple genes. In the case of TTPA gene mutations, NGS can identify specific changes or mutations that may be responsible for vitamin E familial deficiency.

This genetic test not only aids in the diagnosis of individuals with vitamin E familial deficiency, but it can also identify carriers of the condition. Furthermore, it can be utilized for prenatal testing to determine if a fetus has inherited the TTPA gene mutation from their parents.

Genetic testing for TTPA gene mutations is invaluable in providing a definitive diagnosis for individuals suspected of having vitamin E familial deficiency. This diagnosis, in turn, guides appropriate treatment and management strategies.

Contact DNA Labs UAE today to learn more about the TTPA Gene Vitamin E familial deficiency Genetic Test and how it can help diagnose and manage this condition.

Test Name TTPA Gene Vitamin E familial deficiency 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 TTPA Gene Vitamin E familial deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TTPA Gene Vitamin E familial deficiency
Test Details

The TTPA gene is responsible for producing a protein called alpha-tocopherol transfer protein (TTP), which is involved in the transport of vitamin E in the body. Mutations in the TTPA gene can lead to a condition called vitamin E familial deficiency.

Vitamin E familial deficiency is an autosomal recessive disorder characterized by a reduced ability to absorb and transport vitamin E in the body. This can lead to a deficiency of vitamin E, which is an essential antioxidant that protects cells from oxidative damage.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of TTPA gene mutations, NGS can be used to identify specific changes or mutations in the TTPA gene that may be responsible for vitamin E familial deficiency.

NGS genetic testing can help diagnose individuals with vitamin E familial deficiency and identify carriers of the condition. It can also be used for prenatal testing to determine if a fetus has inherited the TTPA gene mutation from their parents.

Genetic testing for TTPA gene mutations can be helpful in providing a definitive diagnosis for individuals with suspected vitamin E familial deficiency and can guide appropriate treatment and management strategies.

SKU: TEST-2104