CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test
At DNA Labs UAE, we offer the CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test to help diagnose and understand this specific type of epilepsy. This test is designed to analyze the CHRNB2 gene, which is associated with the development of epilepsy, particularly the nocturnal frontal lobe type 3 (NFLE3) subtype.
Test Details
NFLE3 is a type of epilepsy that causes seizures during sleep. These seizures are often characterized by sudden movements, vocalizations, and confusion upon awakening. By analyzing the CHRNB2 gene through NGS (next-generation sequencing) technology, our genetic test can identify mutations or variations in the gene that may increase the risk of developing NFLE3 or other forms of epilepsy.
Components and Price
The CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test is priced at 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. The report delivery time is estimated to be 3 to 4 weeks.
Method and Test Type
The test is conducted using NGS technology, which allows for the analysis of multiple genes at once. This comprehensive evaluation of a patient’s genetic profile provides valuable insights into their genetic risk factors for epilepsy and helps inform personalized treatment and management strategies.
Doctor and Test Department
The CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test is recommended for individuals with a family history of epilepsy or those who have experienced seizures during sleep. It is typically ordered by a neurologist and falls under the genetics department.
Pre-Test Information
Prior to undergoing the CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3.
Conclusion
The CHRNB2 Gene Epilepsy Nocturnal Frontal Lobe Type 3 Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing and understanding this specific type of epilepsy. By analyzing the CHRNB2 gene through NGS technology, we can identify genetic risk factors and provide personalized treatment and management strategies for individuals with NFLE3 or other forms of epilepsy.
Test Name | CHRNB2 Gene Epilepsy nocturnal frontal lobe type 3 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 CHRNB2 Gene Epilepsy, nocturnal frontal lobe type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CHRNB2 Gene Epilepsy, nocturnal frontal lobe type 3 |
Test Details |
The CHRNB2 gene is associated with the development of epilepsy, particularly the nocturnal frontal lobe type 3 (NFLE3) subtype. NFLE3 is a type of epilepsy that causes seizures during sleep, often characterized by sudden movements, vocalizations, and confusion upon awakening. NGS (next-generation sequencing) genetic testing is a type of genetic testing that can analyze multiple genes at once, providing a more comprehensive evaluation of a patient’s genetic profile. NGS testing for the CHRNB2 gene can help identify mutations or variations in the gene that may increase the risk of developing NFLE3 or other forms of epilepsy. Individuals with a family history of epilepsy or who have experienced seizures during sleep may benefit from NGS genetic testing to identify potential genetic risk factors and inform personalized treatment and management strategies. |