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TTC8 Gene Bardet-Biedl Syndrome Type 8 Genetic Test

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

-21%

The TTC8 Gene Bardet-Biedl Syndrome Type 8 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the TTC8 gene, which are associated with Bardet-Biedl Syndrome Type 8 (BBS8). Bardet-Biedl Syndrome is a complex genetic condition that affects various parts of the body, including vision, kidney function, obesity, learning disabilities, and abnormalities in the fingers and toes. The test is crucial for individuals with a family history of BBS or those exhibiting symptoms, providing essential information for accurate diagnosis and management of the condition.

Conducted at the state-of-the-art facilities of DNA Labs UAE, the test involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab, which is then analyzed for specific genetic mutations in the TTC8 gene. The process is overseen by qualified geneticists and laboratory technicians, ensuring high accuracy and reliability of the results.

The cost of the TTC8 Gene Bardet-Biedl Syndrome Type 8 Genetic Test is set at 4400 AED. While the price might seem significant, the value of the insights gained from this test cannot be understated, as it not only aids in the diagnosis but also helps in formulating a comprehensive management plan for affected individuals. Early detection through genetic testing can significantly improve the quality of life for patients with Bardet-Biedl Syndrome by allowing for timely interventions and support.

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  • This test is not intended for medical diagnosis or treatment
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TTC8 Gene Bardet-Biedl Syndrome Type 8 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: Hepatology Nephrology Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTC8 Gene Bardet-Biedl Syndrome Type 8 NGS Genetic DNA Test gene TTC8.

Test Details

The TTC8 gene is associated with Bardet-Biedl Syndrome Type 8 (BBS8). Bardet-Biedl Syndrome is a rare genetic disorder characterized by a combination of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and other physical and developmental abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. In the context of Bardet-Biedl Syndrome, NGS genetic testing can be used to identify mutations in the TTC8 gene, which is one of the genes known to be associated with the condition.

By analyzing the DNA sequence of the TTC8 gene, NGS genetic testing can help diagnose Bardet-Biedl Syndrome Type 8 and provide valuable information about the specific genetic changes present in an individual. This information can be used for genetic counseling, family planning, and potentially targeted treatments or interventions.

Test Name TTC8 Gene Bardet-Biedl syndrome type 8 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TTC8 Gene Bardet-Biedl syndrome type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTC8 Gene Bardet-Biedl syndrome type 8 NGS Genetic DNA Test gene TTC8
Test Details

The TTC8 gene is associated with Bardet-Biedl syndrome type 8 (BBS8). Bardet-Biedl syndrome is a rare genetic disorder characterized by a combination of symptoms including obesity, vision problems, kidney abnormalities, intellectual disability, and other physical and developmental abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous sequencing of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. In the context of Bardet-Biedl syndrome, NGS genetic testing can be used to identify mutations in the TTC8 gene, which is one of the genes known to be associated with the condition.

By analyzing the DNA sequence of the TTC8 gene, NGS genetic testing can help diagnose Bardet-Biedl syndrome type 8 and provide valuable information about the specific genetic changes present in an individual. This information can be used for genetic counseling, family planning, and potentially targeted treatments or interventions.

SKU: TEST-3581 Category:

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