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TGFBR1 Gene Marfan Syndrome TGFBR1 Related Genetic Test Cost

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

-21%

The TGFBR1 gene plays a crucial role in the development and maintenance of body tissues. Mutations in the TGFBR1 gene can lead to Marfan Syndrome, a genetic disorder affecting the connective tissue throughout the body. This condition can impact the heart, eyes, blood vessels, and skeleton, leading to a variety of symptoms ranging from mild to life-threatening.

To diagnose Marfan Syndrome related to TGFBR1 gene mutations, genetic testing is available at DNA Labs UAE. This specialized test examines the TGFBR1 gene for specific mutations that are known to cause the disorder. Early detection through this genetic test can enable individuals and their healthcare providers to manage symptoms, monitor potential complications, and implement preventive measures effectively.

The cost of the TGFBR1-related genetic test for Marfan Syndrome at DNA Labs UAE is 4400 AED. This investment can provide invaluable information for affected individuals and their families, guiding clinical decisions and personalized care plans to improve health outcomes and quality of life.

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TGFBR1 Gene Marfan Syndrome Genetic Test

Components:

  • Test Name: TGFBR1 Gene Marfan Syndrome TGFBR1 related Genetic Test
  • 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for TGFBR1 Gene Marfan syndrome, TGFBR1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR1 Gene Marfan syndrome, TGFBR1 related NGS Genetic DNA Test gene TGFBR1.

Test Details:

The TGFBR1 gene is associated with Marfan syndrome, which is a genetic disorder that affects connective tissues in the body. Mutations in the TGFBR1 gene can lead to the development of Marfan syndrome.

TGFBR1-related NGS genetic testing is a type of genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the TGFBR1 gene for any genetic variations or mutations. This test can help in the diagnosis of Marfan syndrome by identifying any pathogenic mutations in the TGFBR1 gene.

NGS technology allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the TGFBR1 gene and other relevant genes associated with Marfan syndrome. This type of genetic testing is highly accurate and can detect both known and novel mutations in the TGFBR1 gene.

By identifying specific mutations in the TGFBR1 gene, TGFBR1-related NGS genetic testing can help in confirming a diagnosis of Marfan syndrome, guiding treatment decisions, and providing information for genetic counseling. It can also be used for carrier testing and prenatal testing in families with a known TGFBR1 mutation.

It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who specializes in genetic disorders. They can provide appropriate counseling and guidance based on the results of the genetic test.

Test Name TGFBR1 Gene Marfan syndrome TGFBR1 related 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TGFBR1 Gene Marfan syndrome, TGFBR1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR1 Gene Marfan syndrome, TGFBR1 related NGS Genetic DNA Test gene TGFBR1
Test Details

The TGFBR1 gene is associated with Marfan syndrome, which is a genetic disorder that affects connective tissues in the body. Mutations in the TGFBR1 gene can lead to the development of Marfan syndrome.

TGFBR1-related NGS genetic testing is a type of genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the TGFBR1 gene for any genetic variations or mutations. This test can help in the diagnosis of Marfan syndrome by identifying any pathogenic mutations in the TGFBR1 gene.

NGS technology allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of the TGFBR1 gene and other relevant genes associated with Marfan syndrome. This type of genetic testing is highly accurate and can detect both known and novel mutations in the TGFBR1 gene.

By identifying specific mutations in the TGFBR1 gene, TGFBR1-related NGS genetic testing can help in confirming a diagnosis of Marfan syndrome, guiding treatment decisions, and providing information for genetic counseling. It can also be used for carrier testing and prenatal testing in families with a known TGFBR1 mutation.

It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who specializes in genetic disorders. They can provide appropriate counseling and guidance based on the results of the genetic test.