SLC2A1 Gene Epilepsy Idiopathic Generalized Type 12 Genetic Test
At DNA Labs UAE, we offer the SLC2A1 Gene Epilepsy idiopathic generalized type 12 Genetic Test for individuals who suspect they may have this condition. This test can provide valuable insights into your genetic makeup and help guide treatment decisions.
Test Components
The SLC2A1 Gene Epilepsy idiopathic generalized type 12 Genetic Test includes the following 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Before undergoing the SLC2A1 Gene Epilepsy idiopathic generalized type 12 Genetic Test, it is recommended to provide the following:
- Clinical History of Patient who is going for SLC2A1 Gene Epilepsy, idiopathic generalized type 12 NGS Genetic DNA Test
- A Genetic Counselling session to draw a pedigree chart of family members affected with SLC2A1 Gene Epilepsy, idiopathic generalized type 12
Test Details
The SLC2A1 gene is responsible for encoding a glucose transporter protein called GLUT1. This protein plays a crucial role in transporting glucose across the blood-brain barrier and into brain cells. Mutations in the SLC2A1 gene have been linked to a rare form of epilepsy known as idiopathic generalized epilepsy type 12 (IGE12).
Individuals with IGE12 typically experience generalized seizures that start in childhood or adolescence and are challenging to control with medication. To confirm a diagnosis of IGE12, NGS genetic testing for SLC2A1 mutations can be conducted. This test involves sequencing the entire SLC2A1 gene to identify any mutations or variations that may contribute to the individual’s symptoms.
By undergoing this type of genetic testing, a more accurate diagnosis can be obtained, leading to better treatment decisions. Treatment options for individuals with a mutation in the SLC2A1 gene may include a ketogenic diet, which is high in fat and low in carbohydrates. This diet has been shown to improve seizure control in individuals with GLUT1 deficiency syndrome, a related condition caused by mutations in the SLC2A1 gene. Other treatment options may involve anticonvulsant medications and/or surgery to remove the affected area of the brain.
At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our SLC2A1 Gene Epilepsy idiopathic generalized type 12 Genetic Test can help individuals understand their condition better and make informed decisions regarding their treatment.
Test Name | SLC2A1 Gene Epilepsy idiopathic generalized type 12 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 SLC2A1 Gene Epilepsy, idiopathic generalized type 12 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SLC2A1 Gene Epilepsy, idiopathic generalized type 12 |
Test Details |
The SLC2A1 gene encodes for a glucose transporter protein known as GLUT1, which is responsible for transporting glucose across the blood-brain barrier and into brain cells. Mutations in the SLC2A1 gene have been associated with a rare form of epilepsy called idiopathic generalized epilepsy type 12 (IGE12). NGS genetic testing for SLC2A1 mutations can be used to confirm a diagnosis of IGE12 in individuals with symptoms of the condition. Symptoms of IGE12 typically include generalized seizures that begin in childhood or adolescence and are difficult to control with medication. NGS genetic testing involves sequencing the entire SLC2A1 gene to identify any mutations or variations that may be contributing to the individual’s symptoms. This type of testing can provide a more accurate diagnosis and help guide treatment decisions. If a mutation in the SLC2A1 gene is identified, treatment may involve a ketogenic diet, which is high in fat and low in carbohydrates, and has been shown to improve seizure control in individuals with GLUT1 deficiency syndrome (a related condition caused by mutations in the SLC2A1 gene). Other treatments may include anticonvulsant medications and/or surgery to remove the affected area of the brain. |