GABRG2 Gene Dravet Syndrome Genetic Test
Components: GABRG2 Gene Dravet Syndrome Genetic Test
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: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for GABRG2 Gene Dravet Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GABRG2 Gene Dravet Syndrome.
Test Details: The GABRG2 gene is associated with Dravet syndrome, a rare genetic disorder that causes seizures in infants and young children. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can identify mutations in the GABRG2 gene and other genes associated with Dravet syndrome. This test involves sequencing the entire coding region of the gene to detect any variations or mutations that may be causing the disorder. This information can help doctors diagnose Dravet syndrome and develop personalized treatment plans for affected individuals.
Test Name | GABRG2 Gene Dravet syndrome Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Neurological Disorders |
Doctor | Neurologist |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for GABRG2 Gene Dravet syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GABRG2 Gene Dravet syndrome |
Test Details | The GABRG2 gene is associated with Dravet syndrome, a rare genetic disorder that causes seizures in infants and young children. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can identify mutations in the GABRG2 gene and other genes associated with Dravet syndrome. This test involves sequencing the entire coding region of the gene to detect any variations or mutations that may be causing the disorder. This information can help doctors diagnose Dravet syndrome and develop personalized treatment plans for affected individuals. |