SCN1A Gene Familial Hemiplegic Migraine Type 3 Genetic Test
Test Name: SCN1A Gene Familial Hemiplegic Migraine Type 3 Genetic Test
Components: DNA Labs UAE
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 SCN1A Gene Familial Hemiplegic Migraine Type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN1A Gene Familial Hemiplegic Migraine Type 3.
Test Details
The SCN1A gene is associated with familial hemiplegic migraine type 3, a rare subtype of migraine that runs in families. This genetic test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the SCN1A gene and identify any mutations or variations that may be associated with this condition.
The test can help diagnose familial hemiplegic migraine type 3 in individuals with symptoms and a family history of the condition, and can also provide valuable information for genetic counseling and family planning. However, it is important to note that not all cases of familial hemiplegic migraine type 3 are caused by mutations in the SCN1A gene, and a negative test result does not necessarily rule out the condition.
Test Name | SCN1A Gene Familial hemiplegic migraine type 3 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 SCN1A Gene Familial hemiplegic migraine type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SCN1A Gene Familial hemiplegic migraine type 3 |
Test Details | The SCN1A gene is associated with familial hemiplegic migraine type 3, a rare subtype of migraine that runs in families. This genetic test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the SCN1A gene and identify any mutations or variations that may be associated with this condition. The test can help diagnose familial hemiplegic migraine type 3 in individuals with symptoms and a family history of the condition, and can also provide valuable information for genetic counseling and family planning. However, it is important to note that not all cases of familial hemiplegic migraine type 3 are caused by mutations in the SCN1A gene, and a negative test result does not necessarily rule out the condition. |