HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24 Genetic Test
Test Name: HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
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 HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HCN1 Gene Early Infantile Epileptic Encephalopathy Type 24.
Test Details: The HCN1 gene is associated with Early Infantile Epileptic Encephalopathy Type 24 (EIEE24), a rare genetic disorder characterized by seizures and developmental delays. The NGS genetic test for this gene can detect mutations or changes in the HCN1 gene that may be responsible for the condition. This test can be used to confirm a diagnosis of EIEE24 and provide information for genetic counseling and family planning. It may also help guide treatment options and management strategies for individuals with the condition.
Test Name | HCN1 Gene Early infantile epileptic encephalopathy type 24 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 HCN1 Gene Early infantile epileptic encephalopathy type 24 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HCN1 Gene Early infantile epileptic encephalopathy type 24 |
Test Details |
The HCN1 gene is associated with Early Infantile Epileptic Encephalopathy Type 24 (EIEE24), a rare genetic disorder characterized by seizures and developmental delays. The NGS genetic test for this gene can detect mutations or changes in the HCN1 gene that may be responsible for the condition. This test can be used to confirm a diagnosis of EIEE24 and provide information for genetic counseling and family planning. It may also help guide treatment options and management strategies for individuals with the condition. |