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FBN1 Gene Marfan Syndrome Genetic Test Cost

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

-21%

The FBN1 gene Marfan Syndrome genetic test is a specialized diagnostic procedure aimed at identifying mutations in the FBN1 gene, which are closely associated with Marfan Syndrome. Marfan Syndrome is a genetic disorder that affects the body’s connective tissue, leading to abnormalities in the heart, blood vessels, bones, joints, and eyes. The FBN1 gene plays a critical role in the production of fibrillin-1, a protein essential for the formation of elastic fibers found in connective tissue.

Conducted at DNA Labs UAE, this test is crucial for individuals with a family history of Marfan Syndrome or those showing symptoms of the condition. Early detection through this genetic test allows for timely management and treatment plans to mitigate the risk of complications such as aortic dissection and vision problems.

The cost of the FBN1 gene Marfan Syndrome genetic test at DNA Labs UAE is 4400 AED. This investment in health provides valuable insights into an individual’s genetic predisposition to Marfan Syndrome, enabling proactive measures for those affected and their families.

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  • This test is not intended for medical diagnosis or treatment
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FBN1 Gene Marfan Syndrome Genetic Test

At DNA Labs UAE, we offer the FBN1 Gene Marfan Syndrome Genetic Test at a cost of AED 4400.0. This test is designed to diagnose Marfan syndrome, a genetic disorder that affects the connective tissue in the body.

Test Components and Price

The FBN1 Gene Marfan Syndrome Genetic Test is priced at AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The test results will be delivered within 3 to 4 weeks.

Method

The FBN1 Gene Marfan Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of an individual’s genes.

Test Type and Doctor

The test falls under the category of Dysmorphology and is conducted by our experienced team of pediatric doctors.

Test Department

The FBN1 Gene Marfan Syndrome Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is essential to provide the clinical history of the patient who will be undergoing the FBN1 Gene Marfan Syndrome NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the FBN1 Gene Marfan Syndrome NGS Genetic DNA Test gene FBN1.

Test Details

The FBN1 gene is specifically associated with Marfan syndrome. NGS genetic testing is a highly advanced method used to analyze an individual’s DNA sequence. In the case of Marfan syndrome, this test helps identify any mutations or variations in the FBN1 gene that may be responsible for the condition. By confirming a diagnosis of Marfan syndrome, this test provides valuable information about the specific genetic changes involved.

Test Name FBN1 Gene Marfan syndrome 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 FBN1 Gene Marfan syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBN1 Gene Marfan syndrome NGS Genetic DNA Test gene FBN1
Test Details

The FBN1 gene is associated with Marfan syndrome, a genetic disorder that affects the connective tissue in the body. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the case of Marfan syndrome, NGS genetic testing can identify any mutations or variations in the FBN1 gene that may be causing the condition. This test can help confirm a diagnosis of Marfan syndrome and provide information about the specific genetic changes involved.