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TGFBR2 Gene Marfan Syndrome TGFBR2 Related Genetic Test Cost

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

-21%

The TGFBR2 gene plays a crucial role in the development and maintenance of body tissues and organs. Mutations in this gene are associated with Marfan syndrome, a genetic disorder that affects the body’s connective tissue, leading to symptoms like tall stature, long limbs, and issues with the cardiovascular, skeletal, and ocular systems.

The TGFBR2-related genetic test is a specialized diagnostic tool designed to detect mutations in the TGFBR2 gene. This test is essential for individuals who exhibit symptoms of Marfan syndrome or have a family history of the condition. Early and accurate diagnosis through genetic testing can enable timely management and treatment, potentially preventing serious complications associated with the syndrome.

At DNA Labs UAE, the TGFBR2 genetic test is available for individuals seeking to confirm a diagnosis of Marfan syndrome or to understand their risk of developing the condition. The test cost is 4400 AED, a worthwhile investment for those needing precise genetic information to guide their healthcare decisions. Conducted in a state-of-the-art laboratory by experienced geneticists, the test ensures reliable results, providing crucial insights into the patient’s genetic health and aiding in the formulation of a personalized treatment plan.

Description

TGFBR2 Gene Marfan syndrome TGFBR2 related Genetic Test

Test Name: TGFBR2 Gene Marfan syndrome TGFBR2 related Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 TGFBR2 Gene Marfan syndrome, TGFBR2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR2 Gene Marfan syndrome, TGFBR2 related NGS Genetic DNA Test gene TGFBR2

Test Details: Marfan syndrome is a genetic disorder that affects the connective tissues in the body. It is caused by mutations in the TGFBR2 gene, which provides instructions for making a protein involved in cell signaling pathways. To diagnose Marfan syndrome and identify TGFBR2 gene mutations, a TGFBR2-related next-generation sequencing (NGS) genetic test can be performed. This test analyzes the DNA sequence of the TGFBR2 gene to identify any genetic variations or mutations that may be causing the disorder. NGS technology allows for the simultaneous analysis of multiple genes, making it an efficient and comprehensive method for genetic testing. It can detect small changes in the DNA sequence, including point mutations, insertions, deletions, and rearrangements. A TGFBR2-related NGS genetic test can help confirm a diagnosis of Marfan syndrome and provide information about the specific genetic mutation involved. This information can be used for genetic counseling, family planning, and potentially guiding treatment decisions.

Test Name	TGFBR2 Gene Marfan syndrome TGFBR2 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 TGFBR2 Gene Marfan syndrome, TGFBR2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR2 Gene Marfan syndrome, TGFBR2 related NGS Genetic DNA Test gene TGFBR2
Test Details	Marfan syndrome is a genetic disorder that affects the connective tissues in the body. It is caused by mutations in the TGFBR2 gene, which provides instructions for making a protein involved in cell signaling pathways. To diagnose Marfan syndrome and identify TGFBR2 gene mutations, a TGFBR2-related next-generation sequencing (NGS) genetic test can be performed. This test analyzes the DNA sequence of the TGFBR2 gene to identify any genetic variations or mutations that may be causing the disorder. NGS technology allows for the simultaneous analysis of multiple genes, making it an efficient and comprehensive method for genetic testing. It can detect small changes in the DNA sequence, including point mutations, insertions, deletions, and rearrangements. A TGFBR2-related NGS genetic test can help confirm a diagnosis of Marfan syndrome and provide information about the specific genetic mutation involved. This information can be used for genetic counseling, family planning, and potentially guiding treatment decisions.