PCDH19 Gene Early infantile epileptic encephalopathy type 9 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 PCDH19 Gene Early infantile epileptic encephalopathy type 9 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PCDH19 Gene Early infantile epileptic encephalopathy type 9.
Test Details
The PCDH19 gene is associated with Early Infantile Epileptic Encephalopathy type 9 (EIEE9), a rare genetic disorder that affects the brain and causes seizures. The condition primarily affects girls and is caused by mutations in the PCDH19 gene located on the X chromosome. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously. This type of testing is useful in identifying mutations in the PCDH19 gene and other genes associated with epilepsy. The PCDH19 gene NGS genetic test involves sequencing the entire coding region of the gene to identify any mutations or variations that may be present. This test can be used to confirm a diagnosis of EIEE9 in individuals with symptoms of the disorder, as well as to identify carriers of the gene mutation in families with a history of the condition. Early diagnosis and treatment of EIEE9 can improve outcomes and quality of life for affected individuals. Genetic testing can also provide valuable information for family planning and genetic counseling.
Test Name | PCDH19 Gene Early infantile epileptic encephalopathy type 9 Genetic Test |
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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 PCDH19 Gene Early infantile epileptic encephalopathy type 9 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PCDH19 Gene Early infantile epileptic encephalopathy type 9 |
Test Details | The PCDH19 gene is associated with Early Infantile Epileptic Encephalopathy type 9 (EIEE9), a rare genetic disorder that affects the brain and causes seizures. The condition primarily affects girls and is caused by mutations in the PCDH19 gene located on the X chromosome. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that analyzes multiple genes simultaneously. This type of testing is useful in identifying mutations in the PCDH19 gene and other genes associated with epilepsy. The PCDH19 gene NGS genetic test involves sequencing the entire coding region of the gene to identify any mutations or variations that may be present. This test can be used to confirm a diagnosis of EIEE9 in individuals with symptoms of the disorder, as well as to identify carriers of the gene mutation in families with a history of the condition. Early diagnosis and treatment of EIEE9 can improve outcomes and quality of life for affected individuals. Genetic testing can also provide valuable information for family planning and genetic counseling. |