KCNB1 Gene Early infantile epileptic encephalopathy type 26 Genetic Test
Test Details
The KCNB1 gene is associated with early infantile epileptic encephalopathy type 26 (EIEE26), a rare genetic disorder characterized by seizures that begin in infancy and developmental delays.
NGS (Next Generation Sequencing) genetic testing can be used to identify mutations in the KCNB1 gene that may be causing EIEE26. This test involves analyzing the patient’s DNA to identify any changes or mutations in the KCNB1 gene.
Identifying the specific mutation in the KCNB1 gene can help with diagnosis and management of EIEE26. Treatment for EIEE26 typically involves antiepileptic medications and supportive therapies to manage symptoms and improve quality of life.
Test Name: KCNB1 Gene Early infantile epileptic encephalopathy type 26 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: Neurological Disorders
- Doctor: Neurologist
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for KCNB1 Gene Early infantile epileptic encephalopathy type 26 NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with KCNB1 Gene Early infantile epileptic encephalopathy type 26
Test Name | KCNB1 Gene Early infantile epileptic encephalopathy type 26 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 KCNB1 Gene Early infantile epileptic encephalopathy type 26 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KCNB1 Gene Early infantile epileptic encephalopathy type 26 |
Test Details |
The KCNB1 gene is associated with early infantile epileptic encephalopathy type 26 (EIEE26), a rare genetic disorder characterized by seizures that begin in infancy and developmental delays. NGS (Next Generation Sequencing) genetic testing can be used to identify mutations in the KCNB1 gene that may be causing EIEE26. This test involves analyzing the patient’s DNA to identify any changes or mutations in the KCNB1 gene. Identifying the specific mutation in the KCNB1 gene can help with diagnosis and management of EIEE26. Treatment for EIEE26 typically involves antiepileptic medications and supportive therapies to manage symptoms and improve quality of life. |