Short Description

NGS genetic DNA test detecets for variant and mutation detection in ATP1A2 gene for Familial hemiplegic migraine type 2

PreTest Information

Clinical History of Patient who is going for ATP1A2 Gene Familial hemiplegic migraine type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ATP1A2 Gene Familial hemiplegic migraine type 2

Detail Description

ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test - Cost, Symptoms, and Diagnosis

Familial Hemiplegic Migraine (FHM) is a rare neurological disorder that is characterized by severe migraine headaches, temporary paralysis on one side of the body, and other neurological symptoms. FHM is caused by mutations in the ATP1A2 gene, which provides instructions for making a protein that is essential for the normal functioning of brain cells.

If you suspect that you or a loved one may have FHM, it is important to get a proper diagnosis. The ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test is a state-of-the-art diagnostic tool that can help identify mutations in the ATP1A2 gene that are associated with FHM.

What is the ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test?

The ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test is a type of genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the DNA of a patient to identify mutations in the ATP1A2 gene. The test is non-invasive and involves collecting a small sample of blood or saliva from the patient.

The test is highly accurate and can identify mutations in the ATP1A2 gene that are associated with FHM. This can help doctors make an accurate diagnosis and provide appropriate treatment for patients.

What are the Symptoms of Familial Hemiplegic Migraine?

Familial Hemiplegic Migraine is characterized by severe migraine headaches that are often accompanied by other neurological symptoms. These symptoms can include:

• Temporary paralysis on one side of the body
• Numbness or tingling on one side of the body
• Difficulty speaking or understanding speech
• Vision changes, such as seeing flashing lights or zigzag lines
• Sensitivity to light and sound
• Nausea and vomiting

These symptoms can last for several hours or even days and can be debilitating for patients. If you experience any of these symptoms, it is important to see a doctor for a proper diagnosis.

How is Familial Hemiplegic Migraine Diagnosed?

Familial Hemiplegic Migraine is diagnosed based on a patient's symptoms and family history. Genetic testing can also be used to confirm a diagnosis. The ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test is a highly accurate diagnostic tool that can help identify mutations in the ATP1A2 gene that are associated with FHM.

What is the Cost of the ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test?

The cost of the ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test in India is approximately INR 20,000. This cost may vary depending on the testing facility and other factors.

Conclusion

Familial Hemiplegic Migraine is a rare neurological disorder that can be debilitating for patients. The ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test is a state-of-the-art diagnostic tool that can help identify mutations in the ATP1A2 gene that are associated with FHM. If you suspect that you or a loved one may have FHM, it is important to see a doctor for a proper diagnosis and to consider genetic testing.

At DNA Labs India, we offer a wide range of genetic testing services, including the ATP1A2 Gene Familial Hemiplegic Migraine Type 2 NGS Genetic DNA Test. Our team of expert geneticists and clinicians are dedicated to providing the highest quality testing and diagnostic services to our patients. Contact us today to learn more about our services and how we can help you.