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OPA3 Gene 3-Methylglutaconic Aciduria Type 3 Genetic Test Cost

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

-21%

The OPA3 Gene 3-Methylglutaconic Aciduria Type 3 Genetic Test is a specialized diagnostic tool designed to identify mutations in the OPA3 gene, which are associated with the rare metabolic disorder known as 3-Methylglutaconic Aciduria Type 3 (MGCA3). This condition is characterized by a spectrum of symptoms, including vision loss, movement disorders, and neurological deficits, which result from the accumulation of 3-methylglutaconic acid and related metabolites in the body due to a deficiency in mitochondrial function.

DNA Labs UAE offers this genetic test as part of its comprehensive suite of diagnostic services, providing a crucial resource for individuals and families seeking answers to complex genetic conditions. By analyzing a sample of the patient’s DNA, the test can confirm the presence of specific mutations in the OPA3 gene, thus aiding in the diagnosis of MGCA3. This information is vital for understanding the risk of disease transmission, guiding treatment decisions, and enabling personalized medical care.

The cost of the OPA3 Gene 3-Methylglutaconic Aciduria Type 3 Genetic Test at DNA Labs UAE is 4400 AED. While the price may be a consideration for some, the value of obtaining a definitive diagnosis and the potential to tailor interventions specifically to an individual’s genetic makeup can be immeasurable for affected families.

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OPA3 Gene 3-methylglutaconic aciduria type 3 Genetic Test

At DNA Labs UAE, we offer the OPA3 Gene 3-methylglutaconic aciduria type 3 Genetic Test at a cost of 4400.0 AED. This test is used to diagnose and identify genetic variants or mutations in the OPA3 gene associated with 3-methylglutaconic aciduria type 3, also known as Costeff syndrome.

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 the OPA3 Gene 3-methylglutaconic aciduria type 3 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with 3-methylglutaconic aciduria type 3.

Test Details

The OPA3 gene is associated with 3-methylglutaconic aciduria type 3, a condition characterized by optic atrophy, movement disorders, developmental delays, and intellectual disability. Our NGS (Next-Generation Sequencing) genetic testing allows for the simultaneous analysis of multiple genes, including the OPA3 gene. NGS technology enables the sequencing of large amounts of DNA in a more efficient and cost-effective manner compared to traditional sequencing methods.

By performing the OPA3 Gene 3-methylglutaconic aciduria type 3 Genetic Test, healthcare professionals can identify any genetic variants or mutations in the OPA3 gene that may be causing the condition. This information can assist with diagnosis, genetic counseling, and potentially guide treatment options or management strategies for the affected individual.

It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics, such as genetic counselors or medical geneticists. They can provide more detailed information and guidance regarding the specific genetic test, its limitations, and the implications of the results.

Test Name OPA3 Gene 3-methylglutaconic aciduria 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 OPA3 Gene 3-methylglutaconic aciduria type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with 3-methylglutaconic aciduria type 3
Test Details

The OPA3 gene is associated with a condition called 3-methylglutaconic aciduria type 3 (also known as Costeff syndrome). This condition is characterized by a variety of symptoms including optic atrophy (degeneration of the optic nerve leading to vision loss), movement disorders, developmental delays, and intellectual disability.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the OPA3 gene. NGS technology enables the sequencing of large amounts of DNA in a more efficient and cost-effective manner compared to traditional sequencing methods.

By performing an NGS genetic test on an individual suspected of having 3-methylglutaconic aciduria type 3, healthcare professionals can identify any genetic variants or mutations in the OPA3 gene that may be causing the condition. This information can help with diagnosis, genetic counseling, and potentially guide treatment options or management strategies for the affected individual.

It is important to note that genetic testing should always be performed and interpreted by qualified healthcare professionals who specialize in genetics, such as genetic counselors or medical geneticists. They can provide more detailed information and guidance regarding the specific genetic test, its limitations, and the implications of the results.