SYN1 Gene Epilepsy X-linked with learning disabilities and behavior disorders Genetic Test
Welcome to DNA Labs UAE, where we offer the SYN1 Gene Epilepsy X-linked with learning disabilities and behavior disorders Genetic Test. This test is designed to identify mutations or changes in the SYN1 gene, using next-generation sequencing (NGS) technology.
Test Details
The SYN1 gene epilepsy, X-linked, with learning disabilities and behavior disorders NGS genetic test is a diagnostic test that helps identify mutations in the SYN1 gene. This gene is responsible for producing a protein called synapsin I. Mutations in this gene can lead to a rare genetic disorder characterized by seizures, learning disabilities, and behavioral problems such as aggression and hyperactivity.
By performing this genetic test, we can confirm a diagnosis of SYN1 gene epilepsy, X-linked, with learning disabilities and behavior disorders. Additionally, the test can also identify carriers of the mutated gene, providing valuable information for family planning and genetic counseling.
Test Components and Price
The SYN1 Gene Epilepsy X-linked with learning disabilities and behavior disorders 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 typically takes 3 to 4 weeks.
Method and Test Type
The test is performed using NGS technology, which allows for rapid and accurate analysis of DNA sequences. It falls under the category of Neurological Disorders, making it an essential tool for neurologists in diagnosing this specific genetic disorder.
Pre Test Information
Prior to undergoing the SYN1 Gene Epilepsy X-linked with learning disabilities and behavior disorders Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by this disorder.
Test Department and Doctor
The SYN1 Gene Epilepsy X-linked with learning disabilities and behavior disorders Genetic Test is conducted in our Genetics department. It is recommended to consult with a Neurologist who specializes in this field.
Conclusion
The SYN1 Gene Epilepsy X-linked with learning disabilities and behavior disorders Genetic Test offered by DNA Labs UAE is a valuable tool in diagnosing and confirming SYN1 gene epilepsy, X-linked, with learning disabilities and behavior disorders. It provides accurate results using NGS technology and helps individuals and families make informed decisions about family planning and genetic counseling.
| Test Name | SYN1 Gene Epilepsy X-linked with learning disabilities and behavior disorders 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 SYN1 Gene Epilepsy, X-linked, with learning disabilities and behavior disorders NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SYN1 Gene Epilepsy, X-linked, with learning disabilities and behavior disorders |
| Test Details |
SYN1 gene epilepsy, X-linked, with learning disabilities and behavior disorders NGS genetic test is a diagnostic test that is used to identify mutations or changes in the SYN1 gene. The test is performed using next-generation sequencing (NGS) technology, which allows for the rapid and accurate analysis of DNA sequences. This genetic test is used to diagnose a rare genetic disorder called SYN1 gene epilepsy, X-linked, with learning disabilities and behavior disorders. This disorder is characterized by seizures, learning disabilities, and behavioral problems such as aggression and hyperactivity. It is caused by mutations in the SYN1 gene, which provides instructions for producing a protein called synapsin I. The SYN1 gene epilepsy, X-linked, with learning disabilities and behavior disorders NGS genetic test can help to confirm a diagnosis of this disorder and can also be used to identify carriers of the mutated gene. This information can be useful for family planning and genetic counseling. The test is performed on a blood sample or other tissue sample and results are typically available within a few weeks. Genetic counseling is recommended for individuals who test positive for the mutated gene. |
