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TGFBR1 Gene Loeys-Dietz Syndrome Type 2A Genetic Test Cost

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

-21%

The TGFBR1 gene Loeys-Dietz syndrome type 2A genetic test is a specialized diagnostic tool designed to identify mutations in the TGFBR1 gene, which are associated with Loeys-Dietz syndrome type 2A. This condition is a rare genetic disorder characterized by the enlargement of the aorta, the large artery that carries blood from the heart to the rest of the body, along with other systemic features including skeletal, skin, and craniofacial abnormalities. Early detection through this test can be crucial for managing the condition, as it allows for timely intervention to prevent serious complications such as aortic dissection.

The test is conducted at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED. DNA Labs UAE employs cutting-edge technology and follows stringent protocols to ensure the accuracy and reliability of the test results. By opting for this test, individuals who have a family history of Loeys-Dietz syndrome or exhibit symptoms related to the condition can gain valuable insights into their genetic makeup, enabling them and their healthcare providers to make informed decisions about their health management and preventive care strategies.

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TGFBR1 Gene Loeys-Dietz Syndrome Type 2A Genetic Test

Components: TGFBR1 Gene Loeys-Dietz syndrome type 2A 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 Loeys-Dietz syndrome type 2A NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR1 Gene Loeys-Dietz syndrome type 2A NGS Genetic DNA Test gene TGFBR1

Test Details: The TGFBR1 gene is a gene that provides instructions for making a protein called transforming growth factor beta receptor 1. This protein is involved in cell signaling pathways that regulate the growth and development of tissues and organs in the body. Loeys-Dietz syndrome type 2A is a rare genetic disorder that affects the connective tissues in the body. It is characterized by features such as aortic aneurysms (weakening and widening of the aorta), arterial tortuosity (twisting and elongation of blood vessels), and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variants that may be associated with a particular condition or disease. A TGFBR1 gene Loeys-Dietz syndrome type 2A NGS genetic test specifically focuses on analyzing the TGFBR1 gene for any genetic variants or mutations that may be associated with Loeys-Dietz syndrome type 2A. This test can help in the diagnosis and management of individuals suspected to have or at risk for this genetic disorder.

Test Name TGFBR1 Gene Loeys-Dietz syndrome type 2A 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 Loeys-Dietz syndrome type 2A NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR1 Gene Loeys-Dietz syndrome type 2A NGS Genetic DNA Test gene TGFBR1
Test Details

The TGFBR1 gene is a gene that provides instructions for making a protein called transforming growth factor beta receptor 1. This protein is involved in cell signaling pathways that regulate the growth and development of tissues and organs in the body.

Loeys-Dietz syndrome type 2A is a rare genetic disorder that affects the connective tissues in the body. It is characterized by features such as aortic aneurysms (weakening and widening of the aorta), arterial tortuosity (twisting and elongation of blood vessels), and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variants that may be associated with a particular condition or disease.

A TGFBR1 gene Loeys-Dietz syndrome type 2A NGS genetic test specifically focuses on analyzing the TGFBR1 gene for any genetic variants or mutations that may be associated with Loeys-Dietz syndrome type 2A. This test can help in the diagnosis and management of individuals suspected to have or at risk for this genetic disorder.