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FBN1 Gene MASS syndrome Genetic Test Cost

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

-21%

The FBN1 Gene MASS Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the FBN1 gene, which are associated with MASS syndrome. MASS syndrome is a connective tissue disorder that shares similarities with Marfan syndrome, affecting the body’s eyes, heart, bones, and skin. The condition is named after its main features: Myopia, Aortic enlargement, Skin and Skeletal abnormalities.

This genetic test is crucial for individuals showing symptoms of MASS syndrome or those with a family history of connective tissue disorders. Early detection through this test can lead to better management and treatment plans, potentially reducing the risk of complications such as aortic dissection.

DNA Labs UAE offers this comprehensive test for a cost of 4400 AED. The process involves collecting a DNA sample, typically through a blood draw, which is then analyzed for mutations in the FBN1 gene. Results from this test can provide valuable information for both patients and healthcare providers, facilitating informed decisions regarding surveillance and management of the condition.

Description

FBN1 Gene MASS Syndrome Genetic Test

Test Name: FBN1 Gene MASS Syndrome Genetic Test

Components: FBN1 gene analysis

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 MASS syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBN1 Gene MASS syndrome NGS Genetic DNA Test gene FBN1

Test Details:

The FBN1 gene is associated with a genetic disorder called MASS syndrome, which stands for Mitral Valve Prolapse, Aortic Aneurysm, Skeletal features, and Skin findings. This syndrome is characterized by abnormalities in the connective tissue, affecting various parts of the body.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of genetic variations or mutations that may be associated with certain disorders or conditions. In the case of MASS syndrome, an NGS genetic test can help identify mutations or variations in the FBN1 gene that may be responsible for the disorder.

By detecting these genetic variations, NGS testing can assist in the diagnosis of MASS syndrome, provide information about the severity of the condition, and help guide treatment decisions. It can also be used for genetic counseling and family planning purposes.

It’s important to note that NGS genetic testing should be performed by a qualified healthcare professional or genetic counselor, as the interpretation of the results requires specialized knowledge and expertise. Additionally, genetic testing may have limitations, and a negative result does not necessarily rule out the presence of a genetic disorder.

Test Name	FBN1 Gene MASS 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 MASS syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBN1 Gene MASS syndrome NGS Genetic DNA Test gene FBN1
Test Details	The FBN1 gene is associated with a genetic disorder called MASS syndrome, which stands for Mitral Valve Prolapse, Aortic Aneurysm, Skeletal features, and Skin findings. This syndrome is characterized by abnormalities in the connective tissue, affecting various parts of the body. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of genetic variations or mutations that may be associated with certain disorders or conditions. In the case of MASS syndrome, an NGS genetic test can help identify mutations or variations in the FBN1 gene that may be responsible for the disorder. By detecting these genetic variations, NGS testing can assist in the diagnosis of MASS syndrome, provide information about the severity of the condition, and help guide treatment decisions. It can also be used for genetic counseling and family planning purposes. It’s important to note that NGS genetic testing should be performed by a qualified healthcare professional or genetic counselor, as the interpretation of the results requires specialized knowledge and expertise. Additionally, genetic testing may have limitations, and a negative result does not necessarily rule out the presence of a genetic disorder.