MTFMT Gene Combined oxidative phosphorylation deficiency type 15 Genetic Test sale cost 4400 AED
SAR1B Gene Chylomicron retention disease Genetic Test sale cost 4400 AED SAR1B Gene Chylomicron retention disease Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
TRMT5 Gene Combined oxidative phosphorylation deficiency type 26 Genetic Test sale cost 4400 AED TRMT5 Gene Combined oxidative phosphorylation deficiency type 26 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!

MTFMT Gene Combined oxidative phosphorylation deficiency type 15 Genetic Test Cost

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

-21%

The MTFMT Gene Combined Oxidative Phosphorylation Deficiency Type 15 Genetic Test is a highly specialized diagnostic tool offered by DNA Labs UAE. This test is specifically designed to identify mutations in the MTFMT gene, which are known to cause Combined Oxidative Phosphorylation Deficiency 15 (COXPD15). COXPD15 is a rare genetic disorder that affects the mitochondrial function, leading to a wide range of clinical manifestations including neurological and muscular impairments.

The testing process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic mutations in the MTFMT gene. The identification of these mutations can provide crucial information for the diagnosis, management, and potential treatment options for individuals affected by COXPD15.

The cost of the MTFMT Gene Combined Oxidative Phosphorylation Deficiency Type 15 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, encompassing the sophisticated techniques and expertise required to accurately identify mutations in the MTFMT gene. Patients considering this test are advised to consult with their healthcare provider to understand its benefits and implications fully.

By offering this genetic test, DNA Labs UAE plays a critical role in advancing the understanding and treatment of mitochondrial disorders, providing patients and their families with essential information for managing the condition.

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

MTFMT Gene Combined oxidative phosphorylation deficiency type 15 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 MTFMT Gene Combined oxidative phosphorylation deficiency type 15 NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with Combined oxidative phosphorylation deficiency type 15

Test Details

MTFMT gene combined oxidative phosphorylation deficiency type 15 is a genetic disorder that affects the mitochondria, which are responsible for producing energy in cells. This disorder is caused by mutations in the MTFMT gene, which is involved in the process of transferring specific molecules to the mitochondria for energy production.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of mutations or variations in specific genes, including the MTFMT gene. This type of testing can help diagnose genetic disorders, including combined oxidative phosphorylation deficiency type 15.

By analyzing the DNA sequence of the MTFMT gene, NGS genetic testing can identify any mutations or variations that may be present. This information can help healthcare professionals diagnose the specific genetic disorder and provide appropriate treatment options or genetic counseling.

It is important to note that NGS genetic testing should be performed by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support.

Test Name MTFMT Gene Combined oxidative phosphorylation deficiency type 15 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 MTFMT Gene Combined oxidative phosphorylation deficiency type 15 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Combined oxidative phosphorylation deficiency type 15
Test Details

MTFMT gene combined oxidative phosphorylation deficiency type 15 is a genetic disorder that affects the mitochondria, which are responsible for producing energy in cells. This disorder is caused by mutations in the MTFMT gene, which is involved in the process of transferring specific molecules to the mitochondria for energy production.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of mutations or variations in specific genes, including the MTFMT gene. This type of testing can help diagnose genetic disorders, including combined oxidative phosphorylation deficiency type 15.

By analyzing the DNA sequence of the MTFMT gene, NGS genetic testing can identify any mutations or variations that may be present. This information can help healthcare professionals diagnose the specific genetic disorder and provide appropriate treatment options or genetic counseling.

It is important to note that NGS genetic testing should be performed by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support.

SKU: TEST-2239 Category:

Related products