MARS2 Gene Combined oxidative phosphorylation deficiency type 25 Genetic Test sale cost 4400 AED
ABHD5 Gene Chanarin-Dorfman syndrome Genetic Test sale cost 4400 AED ABHD5 Gene Chanarin-Dorfman syndrome Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
AARS2 Gene Combined oxidative phosphorylation deficiency type 8 Genetic Test sale cost 4400 AED AARS2 Gene Combined oxidative phosphorylation deficiency type 8 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!

MARS2 Gene Combined oxidative phosphorylation deficiency type 25 Genetic Test Cost

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

-21%

The “MARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 25 Genetic Test” is a specialized diagnostic procedure available at DNA Labs UAE. This test specifically targets the MARS2 gene, which has been linked to Combined Oxidative Phosphorylation Deficiency 25 (COXPD25), a rare genetic disorder. COXPD25 is part of a group of conditions that affect the mitochondrial function, leading to a wide range of symptoms including neurological and muscular impairments, among others. The MARS2 gene plays a crucial role in mitochondrial protein synthesis, and mutations in this gene can disrupt the normal function of mitochondria, leading to the symptoms associated with COXPD25.

The test is designed to identify mutations in the MARS2 gene, providing essential information for accurate diagnosis and management of the condition. It is particularly valuable for families with a history of mitochondrial disorders or unexplained symptoms consistent with mitochondrial dysfunction. Early diagnosis through genetic testing can facilitate timely intervention and management strategies to improve patient outcomes.

The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the MARS2 gene. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, patients can expect high-quality diagnostic processes guided by genetic experts. This test represents a crucial step forward in the personalized care and management of patients with suspected mitochondrial disorders, offering hope for better management of 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

MARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 25 Genetic Test

Welcome to DNA Labs UAE, where we offer the MARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 25 Genetic Test. This diagnostic test is designed to identify variations or mutations in the MARS2 gene, which is responsible for producing the enzyme methionyl-tRNA synthetase 2. This enzyme plays a crucial role in the process of oxidative phosphorylation, which is essential for cellular energy production.

Test Details

The MARS2 gene combined oxidative phosphorylation deficiency type 25 NGS genetic test utilizes next-generation sequencing (NGS) technology to analyze the DNA sequence of the MARS2 gene. By detecting any variations or mutations, this test can aid in the diagnosis of combined oxidative phosphorylation deficiency type 25.

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

Prior to undergoing the MARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 25 NGS Genetic DNA 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 by Combined Oxidative Phosphorylation Deficiency Type 25.

Symptoms and Diagnosis

Individuals who exhibit symptoms of mitochondrial disease, such as muscle weakness, exercise intolerance, developmental delays, and neurological problems, may be recommended to undergo the MARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 25 Genetic Test. This test can also be used for carrier testing in individuals with a family history of Combined Oxidative Phosphorylation Deficiency Type 25.

Interpretation and Importance

It is crucial to note that the MARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 25 Genetic Test is a diagnostic tool that should be interpreted by a healthcare professional or genetic counselor. The results of this test can guide treatment decisions, provide valuable information about the condition’s inheritance pattern, and assess the risk of recurrence.

At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. If you have any questions or would like to schedule a test, please contact us.

Test Name MARS2 Gene Combined oxidative phosphorylation deficiency type 25 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 MARS2 Gene Combined oxidative phosphorylation deficiency type 25 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Combined oxidative phosphorylation deficiency type 25
Test Details

MARS2 gene combined oxidative phosphorylation deficiency type 25 NGS genetic test is a diagnostic test that looks for variations or mutations in the MARS2 gene. This gene is responsible for providing instructions to produce an enzyme called methionyl-tRNA synthetase 2, which is involved in the process of oxidative phosphorylation.

Oxidative phosphorylation is a crucial process in the production of cellular energy in the form of adenosine triphosphate (ATP). Mutations in the MARS2 gene can lead to a deficiency in oxidative phosphorylation, resulting in a condition known as combined oxidative phosphorylation deficiency type 25.

This genetic test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the MARS2 gene and identify any variations or mutations. By detecting these genetic changes, the test can help in the diagnosis of combined oxidative phosphorylation deficiency type 25.

The test may be recommended for individuals who exhibit symptoms of mitochondrial disease, such as muscle weakness, exercise intolerance, developmental delays, and neurological problems. It can also be used for carrier testing in individuals with a family history of combined oxidative phosphorylation deficiency type 25.

It is important to note that this genetic test is a diagnostic tool and should be interpreted by a healthcare professional or genetic counselor. The results of the test can help guide treatment decisions and provide valuable information about the condition’s inheritance pattern and recurrence risk.

SKU: TEST-2250 Category:

Related products