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TGFBR2 Gene Loeys-Dietz Syndrome Type 1B Genetic Test Cost

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

-21%

The TGFBR2 Gene Loeys-Dietz Syndrome Type 1B Genetic Test is a specialized diagnostic tool designed to detect mutations in the TGFBR2 gene, which are associated with Loeys-Dietz Syndrome Type 1B (LDS1B). Loeys-Dietz Syndrome 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 manifestations including skeletal, skin, and craniofacial abnormalities. Early detection through genetic testing is crucial for managing the condition, as it can lead to life-threatening complications if left untreated.

The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics and research. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis, which includes the collection of a DNA sample, usually through a blood draw or a cheek swab, followed by detailed laboratory analysis to identify any mutations in the TGFBR2 gene. Results from this test can provide invaluable information for affected individuals and their families, including insights into the risk of developing the syndrome, guidance for clinical management, and the potential for targeted treatments. Given the complexities and potential severity of Loeys-Dietz Syndrome, this genetic test represents a critical step in proactive health care and personalized medicine.

Description

TGFBR2 Gene Loeys-Dietz Syndrome Type 1B Genetic Test

Test Name: TGFBR2 Gene Loeys-Dietz syndrome type 1B Genetic Test

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

Price: 4400.0 AED

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 Loeys-Dietz syndrome type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR2 Gene Loeys-Dietz syndrome type 1B NGS Genetic DNA Test gene TGFBR2

Test Details: The TGFBR2 gene is associated with a genetic disorder called Loeys-Dietz syndrome type 1B. This syndrome is characterized by various abnormalities of the connective tissues in the body, including the heart, blood vessels, and skeletal system.

NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Loeys-Dietz syndrome type 1B, NGS genetic testing can be used to identify any mutations or variations in the TGFBR2 gene that may be responsible for the syndrome. By analyzing the TGFBR2 gene, NGS genetic testing can help diagnose Loeys-Dietz syndrome type 1B and provide valuable information for medical management and treatment options. It can also help identify individuals who may be at risk of passing the condition on to their children.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.

Test Name	TGFBR2 Gene Loeys-Dietz syndrome type 1B 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 Loeys-Dietz syndrome type 1B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TGFBR2 Gene Loeys-Dietz syndrome type 1B NGS Genetic DNA Test gene TGFBR2
Test Details	The TGFBR2 gene is associated with a genetic disorder called Loeys-Dietz syndrome type 1B. This syndrome is characterized by various abnormalities of the connective tissues in the body, including the heart, blood vessels, and skeletal system. NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Loeys-Dietz syndrome type 1B, NGS genetic testing can be used to identify any mutations or variations in the TGFBR2 gene that may be responsible for the syndrome. By analyzing the TGFBR2 gene, NGS genetic testing can help diagnose Loeys-Dietz syndrome type 1B and provide valuable information for medical management and treatment options. It can also help identify individuals who may be at risk of passing the condition on to their children. It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.