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TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test Cost

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

-21%

The TSFM gene is associated with a rare condition known as Combined Oxidative Phosphorylation Deficiency Type 3 (COXPD3). This genetic disorder affects the body’s ability to produce energy efficiently, leading to a range of symptoms that can include muscle weakness, heart problems, and developmental delays, among others. The condition is inherited in an autosomal recessive pattern, meaning that a child must inherit two copies of the mutated gene, one from each parent, to be affected.

To diagnose this condition, a specific genetic test targeting the TSFM gene can be performed. This test looks for mutations in the TSFM gene that are known to cause Combined Oxidative Phosphorylation Deficiency Type 3. It is a crucial step in confirming the diagnosis, understanding the disease’s progression, and exploring potential treatment options.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic testing service. The cost of the TSFM gene test is 4400 AED. Conducting this test at DNA Labs UAE ensures that individuals and families receive accurate and comprehensive results, thanks to the lab’s expertise in genetic diagnostics and its use of advanced testing technologies. This information is vital for affected families to make informed decisions about their health and to seek appropriate medical interventions.

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TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test

At DNA Labs UAE, we offer the TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test to help diagnose and understand this genetic disorder. This test is designed to identify mutations in the TSFM gene, which is responsible for mitochondrial function and energy production in cells.

Test Details

TSFM Gene Combined Oxidative Phosphorylation Deficiency Type 3 is a genetic disorder that affects the function of mitochondria, which are responsible for producing energy in cells through a process called oxidative phosphorylation. This disorder is caused by mutations in the TSFM gene, which provides instructions for making a protein called mitochondrial translation elongation factor Ts (Tsfm).

A NGS (Next-Generation Sequencing) genetic test can be used to identify mutations in the TSFM gene. This test involves sequencing the DNA of an individual to detect any changes or variations in the gene sequence. By analyzing the TSFM gene, the test can determine if there are any mutations that may be causing or contributing to the combined oxidative phosphorylation deficiency type 3 disorder.

The NGS genetic test can help in diagnosing individuals with this disorder, as well as identifying carriers of the TSFM gene mutation. It can also provide information about the specific mutation present, which can be helpful in determining the prognosis and potential treatment options for affected individuals.

Test Components and Price

The TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test is available at a cost of 4400.0 AED.

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA Card for this test.

Report Delivery

The test results will be delivered within 3 to 4 weeks after sample submission.

Method

We use NGS Technology for the TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test.

Test Type

This test falls under the category of Metabolic Disorders.

Doctor

Our dedicated team of General Physicians will assist you throughout the testing process.

Test Department

The TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is recommended to provide the clinical history of the patient who is going for the TSFM Gene Combined oxidative phosphorylation deficiency type 3 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with Combined oxidative phosphorylation deficiency type 3.

Conclusion

It is important to consult with a healthcare professional or a genetic counselor to understand the implications of the test results and to discuss any further steps or recommendations based on the findings. At DNA Labs UAE, we are committed to providing reliable and accurate genetic testing services to assist in the diagnosis and management of genetic disorders.

Test Name TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TSFM Gene Combined oxidative phosphorylation deficiency type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Combined oxidative phosphorylation deficiency type 3
Test Details

TSFM Gene Combined Oxidative Phosphorylation Deficiency Type 3 is a genetic disorder that affects the function of mitochondria, which are responsible for producing energy in cells through a process called oxidative phosphorylation. This disorder is caused by mutations in the TSFM gene, which provides instructions for making a protein called mitochondrial translation elongation factor Ts (Tsfm).

A NGS (Next-Generation Sequencing) genetic test can be used to identify mutations in the TSFM gene. This test involves sequencing the DNA of an individual to detect any changes or variations in the gene sequence. By analyzing the TSFM gene, the test can determine if there are any mutations that may be causing or contributing to the combined oxidative phosphorylation deficiency type 3 disorder.

The NGS genetic test can help in diagnosing individuals with this disorder, as well as identifying carriers of the TSFM gene mutation. It can also provide information about the specific mutation present, which can be helpful in determining the prognosis and potential treatment options for affected individuals.

It is important to consult with a healthcare professional or a genetic counselor to understand the implications of the test results and to discuss any further steps or recommendations based on the findings.

SKU: TEST-2252 Category:

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