DCX Gene Lissencephaly/Subcortical Laminal Heteropia X-Linked Genetic Test
Introduction
DCX gene lissencephaly/subcortical laminal heterotopia, X-linked is a genetic disorder that affects brain development. It is caused by mutations in the DCX gene, which is located on the X chromosome.
Test Details
Test Name: DCX Gene Lissencephaly/Subcortical Laminal Heteropia X-Linked Genetic Test
Components: DCX gene analysis
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 DCX Gene Lissencephaly/Subcortical Laminal Heteropia, X-linked NGS Genetic DNA Test
A Genetic Counselling session to draw a pedigree chart of family members affected with DCX Gene Lissencephaly/Subcortical Laminal Heteropia, X-linked
Test Description
Next-generation sequencing (NGS) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic mutations. In the case of DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, NGS genetic testing can be used to detect mutations in the DCX gene.
NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This allows for the identification of genetic variations and mutations that may be associated with the disorder.
Benefits of the Test
By performing NGS genetic testing for DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, healthcare professionals can diagnose the condition and provide appropriate genetic counseling and management options for affected individuals and their families.
Test Name | DCX Gene LissencephalySubcortical laminal heteropia X-linked 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 DCX Gene Lissencephaly/Subcortical laminal heteropia, X-linked NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DCX Gene Lissencephaly/Subcortical laminal heteropia, X-linked |
Test Details | DCX gene lissencephaly/subcortical laminal heterotopia, X-linked is a genetic disorder that affects brain development. It is caused by mutations in the DCX gene, which is located on the X chromosome. Next-generation sequencing (NGS) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic mutations. In the case of DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, NGS genetic testing can be used to detect mutations in the DCX gene. NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This allows for the identification of genetic variations and mutations that may be associated with the disorder. By performing NGS genetic testing for DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, healthcare professionals can diagnose the condition and provide appropriate genetic counseling and management options for affected individuals and their families. |