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MSX2 Gene Parietal Foramina Type 1 Genetic Test Cost

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

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The “MSX2 Gene Parietal Foramina Type 1 Genetic Test” is a specialized diagnostic tool designed to identify mutations in the MSX2 gene, which are associated with Parietal Foramina Type 1, a rare genetic condition. This condition is characterized by the incomplete closure of the bones in the skull, leading to parietal foramina, or small holes in the parietal bones. These can vary in size and are sometimes associated with other clinical symptoms, though many individuals may remain asymptomatic.

The test is performed at DNA Labs UAE, a facility known for its advanced genetic testing capabilities. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed to detect any mutations in the MSX2 gene that indicate the presence of Parietal Foramina Type 1. This genetic test is crucial for accurate diagnosis, allowing for appropriate monitoring and management of the condition.

The cost of the MSX2 Gene Parietal Foramina Type 1 Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem high, the test provides invaluable information for affected individuals and their families, enabling them to understand their genetic condition better and make informed decisions about their health and care.

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MSX2 Gene Parietal foramina type 1 Genetic Test

Are you looking for information about the MSX2 Gene Parietal foramina type 1 Genetic Test? DNA Labs UAE is here to provide you with all the details you need.

Test Components and Price

The MSX2 Gene Parietal foramina type 1 Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Symptoms and Diagnosis

Parietal foramina type 1 (PFM1) is a rare genetic condition characterized by small holes in the parietal bones of the skull. The MSX2 gene is responsible for this condition. Our genetic test uses Next-Generation Sequencing (NGS) technology to identify any mutations or genetic variants in the MSX2 gene, helping to confirm a diagnosis of PFM1. This test can also be used for carrier testing in individuals with a family history of the condition.

Test Details

The MSX2 gene parietal foramina type 1 NGS genetic test involves sequencing the entire coding region of the MSX2 gene to identify any genetic variants or mutations that may be present. This information is crucial for genetic counseling, family planning, and the management of individuals affected by PFM1. Furthermore, understanding the underlying genetic mechanisms of the condition can aid in the development of potential targeted treatments in the future.

Report Delivery and Pre-Test Information

The report for the MSX2 Gene Parietal foramina type 1 Genetic Test will be delivered within 3 to 4 weeks. Before the test, it is important to provide the clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected by PFM1.

Doctor and Test Department

This genetic test is conducted by a doctor specializing in pediatrics. The test is performed in the Genetics department of DNA Labs UAE.

By choosing the MSX2 Gene Parietal foramina type 1 Genetic Test, you can gain valuable insights into your genetic makeup and make informed decisions regarding your health and family planning. Contact DNA Labs UAE today to schedule your test.

Test Name MSX2 Gene Parietal foramina type 1 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MSX2 Gene Parietal foramina type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MSX2 Gene Parietal foramina type 1 NGS Genetic DNA Test gene MSX2
Test Details

MSX2 gene parietal foramina type 1 NGS genetic test is a genetic test that is used to identify mutations in the MSX2 gene associated with parietal foramina type 1 (PFM1). PFM1 is a rare genetic condition characterized by the presence of small holes (foramina) in the parietal bones of the skull. This condition is caused by mutations in the MSX2 gene, which plays a critical role in the development of the skull and facial bones.

The NGS (Next-Generation Sequencing) genetic test involves sequencing the entire coding region of the MSX2 gene to identify any genetic variants or mutations that may be present. This test can help in confirming a diagnosis of PFM1 and can also be used for carrier testing in individuals with a family history of the condition.

Identifying the specific mutation in the MSX2 gene can provide valuable information for genetic counseling, family planning, and management of individuals affected by PFM1. It can also aid in understanding the underlying genetic mechanisms of the condition, which may help in developing potential targeted treatments in the future.

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