GABRB3 Gene Epilepsy Childhood Absence Type 5 Genetic Test
Test Name: GABRB3 Gene Epilepsy Childhood Absence Type 5 Genetic Test
Components: NGS Technology
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for GABRB3 Gene Epilepsy, Childhood Absence Type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GABRB3 Gene Epilepsy, Childhood Absence Type 5.
Test Details
The GABRB3 gene is associated with epilepsy, specifically childhood absence type 5. Childhood absence epilepsy is a type of seizure disorder that typically begins in early childhood and is characterized by brief episodes of staring or loss of awareness.
NGS genetic testing can identify mutations or variations in the GABRB3 gene that may contribute to the development of childhood absence epilepsy. This type of testing involves sequencing the DNA in the GABRB3 gene to look for any abnormalities that may be causing the disorder.
Knowing whether a person has a mutation or variation in the GABRB3 gene can help with diagnosis and treatment of childhood absence epilepsy. It can also provide information about the risk of passing the condition on to future generations.
It is important to note that genetic testing is not always necessary or appropriate for every person with childhood absence epilepsy. A healthcare provider can help determine if genetic testing is necessary and provide counseling about the potential benefits and risks of testing.
| Test Name | GABRB3 Gene Epilepsy childhood absence type 5 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 GABRB3 Gene Epilepsy, childhood absence type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GABRB3 Gene Epilepsy, childhood absence type 5 |
| Test Details |
The GABRB3 gene is associated with epilepsy, specifically childhood absence type 5. Childhood absence epilepsy is a type of seizure disorder that typically begins in early childhood and is characterized by brief episodes of staring or loss of awareness. NGS genetic testing can identify mutations or variations in the GABRB3 gene that may contribute to the development of childhood absence epilepsy. This type of testing involves sequencing the DNA in the GABRB3 gene to look for any abnormalities that may be causing the disorder. Knowing whether a person has a mutation or variation in the GABRB3 gene can help with diagnosis and treatment of childhood absence epilepsy. It can also provide information about the risk of passing the condition on to future generations. It is important to note that genetic testing is not always necessary or appropriate for every person with childhood absence epilepsy. A healthcare provider can help determine if genetic testing is necessary and provide counseling about the potential benefits and risks of testing. |
