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SCN1A Gene Familial Hemiplegic Migraine Type 3 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The SCN1A Gene Familial Hemiplegic Migraine Type 3 Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to detect mutations in the SCN1A gene, which have been associated with Familial Hemiplegic Migraine Type 3 (FHM3). Familial Hemiplegic Migraine is a rare subtype of migraine with aura, characterized by temporary paralysis on one side of the body, visual disturbances, and sometimes speech difficulties before the onset of headache. The SCN1A gene plays a crucial role in the functioning of nerve cells in the brain, and mutations in this gene can disrupt ion channels, leading to the symptoms of FHM3.

This genetic test is crucial for individuals with a family history of FHM3, as it can provide definitive confirmation of the mutation presence, aiding in the accurate diagnosis and management of the condition. The test involves a simple blood draw or cheek swab, with the sample then analyzed for specific genetic mutations in the SCN1A gene.

The cost of the SCN1A Gene Familial Hemiplegic Migraine Type 3 Genetic Test at DNA Labs UAE is 4400 AED. Given the specialized nature of this test and its importance in the precise diagnosis and potential treatment strategies for individuals with or at risk of FHM3, the investment can be invaluable for affected families seeking clarity on their genetic status and how it may impact their health management plans.

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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.