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PEX3 Gene Peroxisome Biogenesis Disorder Type 10A Genetic Test Cost

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

-21%

The “PEX3 Gene Peroxisome Biogenesis Disorder Type 10A Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the PEX3 gene. These mutations are associated with Peroxisome Biogenesis Disorder Type 10A (PBD10A), a rare genetic condition that affects the body’s ability to produce peroxisomes. Peroxisomes are essential for various cellular functions, including lipid metabolism and the detoxification of harmful substances.

This genetic test is critical for early detection and management of PBD10A, enabling healthcare providers to develop a tailored treatment plan for affected individuals. The test involves collecting a DNA sample, typically through a blood draw, and analyzing the genetic material for specific mutations in the PEX3 gene.

Offered at a cost of 4400 AED, the test is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. The test’s accuracy and the lab’s reputation make it a valuable resource for families with a history of PBD10A or related symptoms, providing them with crucial information about their genetic health and guiding future medical decisions.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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PEX3 Gene Peroxisome biogenesis disorder type 10A Genetic Test

Are you looking for a genetic test for PEX3 Gene Peroxisome biogenesis disorder type 10A? DNA Labs UAE offers the PEX3 Gene Peroxisome biogenesis disorder type 10A Genetic Test at a cost of 4400.0 AED.

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

Before undergoing the PEX3 Gene Peroxisome biogenesis disorder type 10A 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 PEX3 Gene Peroxisome biogenesis disorder type 10A.

Test Details

The PEX3 gene is associated with a rare genetic disorder called peroxisome biogenesis disorder type 10A (PBD10A). This disorder is characterized by the impaired development and functioning of peroxisomes, which are cellular structures involved in various metabolic processes.

The PEX3 Gene Peroxisome biogenesis disorder type 10A Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. This advanced sequencing technology can identify mutations or variations in the PEX3 gene that may be responsible for the disorder.

By analyzing the PEX3 gene, the NGS genetic test can provide valuable information about the specific genetic changes present in an individual’s DNA. This information is crucial for diagnosing PBD10A, predicting the severity of the condition, guiding treatment decisions, and providing genetic counseling to affected individuals and their families.

It is important to note that NGS genetic testing should be performed by healthcare professionals, such as geneticists or genetic counselors. The results of the test should be interpreted in the context of an individual’s clinical symptoms and family history.

Don’t delay in getting the PEX3 Gene Peroxisome biogenesis disorder type 10A Genetic Test. Contact DNA Labs UAE today to schedule your test and gain valuable insights into your genetic health.

Test Name PEX3 Gene Peroxisome biogenesis disorder type 10A 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 PEX3 Gene Peroxisome biogenesis disorder type 10A NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PEX3 Gene Peroxisome biogenesis disorder type 10A
Test Details

PEX3 gene is associated with a condition called peroxisome biogenesis disorder type 10A (PBD10A). PBD10A is a rare genetic disorder characterized by the impaired development and functioning of peroxisomes, which are cellular structures involved in various metabolic processes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of PBD10A, NGS genetic testing can identify mutations or variations in the PEX3 gene that may be responsible for the disorder.

By analyzing the PEX3 gene, NGS genetic testing can provide information about the specific genetic changes present in an individual’s DNA. This information can help in diagnosing PBD10A, predicting the severity of the condition, guiding treatment decisions, and providing genetic counseling to affected individuals and their families.

It’s important to note that NGS genetic testing is typically performed by healthcare professionals, such as geneticists or genetic counselors, and the results should be interpreted in the context of an individual’s clinical symptoms and family history.

SKU: TEST-1906 Category:

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