SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy Genetic Test
At DNA Labs UAE, we offer the SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy Genetic Test at a cost of AED 4400.0. This test is specifically designed to diagnose individuals with suspected Leukoencephalopathy with dystonia and motor neuropathy (LDMN) by analyzing the SCP2 gene using NGS (Next-Generation Sequencing) technology.
Test Components and Price
The SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy Genetic Test includes the following components:
- 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
The cost of the test is AED 4400.0.
Pre Test Information
Before undergoing the SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy 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 with LDMN. This information helps in providing accurate results and guidance for treatment and family planning.
About Leukoencephalopathy with dystonia and motor neuropathy (LDMN)
LDMN is a rare neurodegenerative disorder characterized by progressive dystonia, motor neuropathy, and leukoencephalopathy. Individuals with LDMN experience involuntary muscle contractions, damage to the nerves controlling movement, and abnormalities in the white matter of the brain.
NGS Genetic Testing for LDMN
NGS genetic testing is a powerful technique used to analyze multiple genes simultaneously to identify mutations or variations associated with genetic disorders. In the case of LDMN, NGS testing can specifically identify mutations or variations in the SCP2 gene that may be responsible for the disorder.
By analyzing the SCP2 gene using NGS, healthcare professionals can provide a definitive diagnosis for individuals suspected of having LDMN. This diagnosis is crucial for guiding treatment decisions, providing genetic counseling, and assisting in family planning.
Research and Future Developments
NGS testing for LDMN not only aids in diagnosis and treatment decisions but also contributes to ongoing research efforts. By understanding the genetic basis of LDMN through NGS testing, researchers can potentially develop targeted therapies in the future.
At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy Genetic Test offers a comprehensive analysis that can make a significant impact on the lives of individuals and families affected by LDMN.
Test Name | SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy 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 SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SCP2 Gene Leukoencephalopathy with dystonia and motor neuropathy |
Test Details |
The SCP2 gene is associated with a rare genetic disorder called Leukoencephalopathy with dystonia and motor neuropathy (LDMN). LDMN is a neurodegenerative disorder characterized by a combination of symptoms including progressive dystonia (involuntary muscle contractions), motor neuropathy (damage to the nerves that control movement), and leukoencephalopathy (abnormalities in the white matter of the brain). NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously to identify mutations or variations that may be responsible for a particular genetic disorder. In the case of LDMN, NGS genetic testing can be used to identify mutations or variations in the SCP2 gene that may be causing the disorder. By analyzing the SCP2 gene using NGS, healthcare professionals can provide a definitive diagnosis for individuals with suspected LDMN. This can help guide treatment decisions and provide important information for genetic counseling and family planning. Additionally, NGS testing can also be used for research purposes to further understand the genetic basis of LDMN and potentially develop targeted therapies in the future. |