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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 offered at DNA Labs UAE, designed to identify mutations in the FBN1 gene, which are associated with Marfan syndrome. Marfan syndrome is a genetic disorder that affects the body’s connective tissue, leading to symptoms in various systems, including the skeletal, cardiovascular, and ocular systems. The test is crucial for individuals with a family history of Marfan syndrome or those exhibiting symptoms, as early detection can lead to better management and treatment of the condition. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to accurately interpret the results. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test provides individuals and families with essential information for making informed health decisions.

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
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FBN1 Gene Marfan Syndrome Genetic Test

At DNA Labs UAE, we offer the FBN1 Gene Marfan Syndrome Genetic Test for individuals who may be at risk of Marfan syndrome. Marfan syndrome is a genetic disorder that affects the connective tissues in the body. Our advanced NGS (Next-Generation Sequencing) technology allows for a comprehensive analysis of the FBN1 gene, which is associated with Marfan syndrome.

Test Components

The FBN1 Gene Marfan Syndrome Genetic Test includes:

  • NGS Technology
  • Cardiovascular Pneumology Disorders Test Type
  • Genetics Test Department

Price

The cost of the FBN1 Gene Marfan Syndrome Genetic Test is 4400.0 AED.

Sample Condition

We accept the following sample conditions:

  • Blood
  • Extracted DNA
  • One drop Blood on FTA Card

Report Delivery

Reports will be delivered within 3 to 4 weeks after the sample is received.

Method

The FBN1 Gene Marfan Syndrome Genetic Test utilizes NGS (Next-Generation Sequencing) technology for accurate and comprehensive analysis.

Test Type

This test focuses on Cardiovascular Pneumology Disorders.

Doctor

A Cardiologist will oversee the FBN1 Gene Marfan Syndrome Genetic Test.

Test Department

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

Pre Test Information

Prior to the test, it is important to provide the clinical history of the patient who is going for the FBN1 Gene Marfan Syndrome Genetic Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the FBN1 Gene Marfan Syndrome Genetic Test gene (FBN1).

Test Details

The FBN1 gene is associated with Marfan syndrome, a genetic disorder that affects connective tissues in the body. The NGS (Next-Generation Sequencing) technology used in this test allows for the analysis of the FBN1 gene for mutations or variations that may be linked to Marfan syndrome. By sequencing the DNA of an individual, we can identify any changes in the FBN1 gene that may be causing the symptoms associated with Marfan syndrome. This comprehensive analysis can aid in the diagnosis and management of Marfan syndrome, as well as provide valuable information for genetic counseling and family planning.

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 Cardiovascular Pneumology Disorders
Doctor Cardiologist
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 connective tissues in the body. NGS (Next-Generation Sequencing) is a type of genetic test that can be used to analyze the FBN1 gene for mutations or variations that may be linked to Marfan syndrome. This test involves sequencing the DNA of an individual to identify any changes in the FBN1 gene that may be causing the symptoms associated with Marfan syndrome. NGS technology allows for the simultaneous analysis of multiple genes or even the entire exome or genome, providing a comprehensive view of an individual’s genetic makeup. This can help in the diagnosis and management of Marfan syndrome, as well as providing valuable information for genetic counseling and family planning.