Sale!

TSC1 and TSC2 Gene Analysis Test Cost

Original price was: 9,600 د.إ.Current price is: 7,200 د.إ.

-25%

The TSC1 and TSC2 Gene Analysis Test is a comprehensive genetic screening procedure aimed at identifying mutations in the TSC1 and TSC2 genes, which are known to cause tuberous sclerosis complex (TSC). TSC is a genetic disorder that can lead to the development of benign tumors in various parts of the body, including the brain, skin, heart, eyes, kidneys, and lungs. Early detection through this test can aid in the management and treatment of the condition, potentially improving the quality of life for those affected.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw, from the individual. The laboratory then uses advanced genetic sequencing techniques to analyze the TSC1 and TSC2 genes for any mutations that are associated with the disorder.

The cost of the TSC1 and TSC2 Gene Analysis Test at DNA Labs UAE is 7200 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in these specific genes. Given the potential impact on patient care and the complexity of the genetic analysis involved, this test represents a valuable tool for individuals at risk of tuberous sclerosis complex or those seeking a definitive diagnosis following the presentation of symptoms.

Description

TSC1 and TSC2 Gene Analysis Test

Test Name: TSC1 and TSC2 Gene Analysis Test

Components: Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer (3 ml)

Price: 7200.0 AED

Sample Condition: Amniotic fluid/ Chorionic villi/ Peripheral blood

Report Delivery: 4-6 weeks

Method: NGS (Next-Generation Sequencing)

Test Type: Genetics

Doctor: General Physician

Test Department: DNA Labs UAE

Pre Test Information: TSC1 & TSC2 Gene Analysis can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details: TSC1 and TSC2 are two genes that are associated with the development of tuberous sclerosis complex (TSC), a rare genetic disorder that affects multiple organ systems. TSC1 is located on chromosome 9 and encodes a protein called hamartin, while TSC2 is located on chromosome 16 and encodes a protein called tuberin. Both proteins are involved in regulating cell growth and division.

Analysis of the TSC1 and TSC2 genes can be done through genetic testing, which involves examining a person’s DNA for mutations or changes in the genes that may be associated with TSC. This testing can be done through a blood or saliva sample and can help diagnose TSC in individuals who have symptoms or a family history of the condition.

In addition to diagnosing TSC, genetic testing can also be used to identify carriers of TSC mutations, which can be helpful for family planning and genetic counseling. It can also provide information about the severity of the condition and potential complications.

Overall, TSC1 and TSC2 gene analysis plays an important role in the diagnosis, management, and understanding of tuberous sclerosis complex.

Test Name	TSC1 and TSC2 Gene Analysis Test
Components	Sterile container/ Sterile Normal Saline Container/ EDTA Vacutainer (3 ml)
Price	7200.0 AED
Sample Condition	Amniotic fluid\/ Chorionic villi\/ Peripheral blood
Report Delivery	4-6 weeks
Method	NGS
Test type	Genetics
Doctor	General Physician
Test Department:
Pre Test Information	TSC1 & TSC2 Gene Analysis can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details	TSC1 and TSC2 are two genes that are associated with the development of tuberous sclerosis complex (TSC), a rare genetic disorder that affects multiple organ systems. TSC1 is located on chromosome 9 and encodes a protein called hamartin, while TSC2 is located on chromosome 16 and encodes a protein called tuberin. Both proteins are involved in regulating cell growth and division. Analysis of the TSC1 and TSC2 genes can be done through genetic testing, which involves examining a person’s DNA for mutations or changes in the genes that may be associated with TSC. This testing can be done through a blood or saliva sample and can help diagnose TSC in individuals who have symptoms or a family history of the condition. In addition to diagnosing TSC, genetic testing can also be used to identify carriers of TSC mutations, which can be helpful for family planning and genetic counseling. It can also provide information about the severity of the condition and potential complications. Overall, TSC1 and TSC2 gene analysis plays an important role in the diagnosis, management, and understanding of tuberous sclerosis complex.