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DEPDC5 Gene Epilepsy familial focal with variable foci Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The DEPDC5 gene plays a significant role in the development of familial focal epilepsy with variable foci, a complex form of epilepsy characterized by seizures originating in different parts of the brain. This condition is inherited in an autosomal dominant pattern, meaning a mutation in just one of the two copies of the gene is sufficient to increase the risk of developing epilepsy.

DNA Labs UAE offers a specialized genetic test to identify mutations in the DEPDC5 gene, providing essential information for families affected by this condition. The test is crucial for accurate diagnosis, understanding the risk of transmission to offspring, and guiding treatment decisions. The cost of the test is 4400 AED, making it a valuable investment for families seeking insights into their genetic predisposition to familial focal epilepsy with variable foci. This test is a step forward in personalized medicine, allowing for tailored treatment plans based on genetic makeup.

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DEPDC5 Gene Epilepsy Familial Focal with Variable Foci Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab in the UAE. We offer the DEPDC5 Gene Epilepsy familial focal with variable foci Genetic Test at a cost of AED 4400.0.

Test Details

The DEPDC5 gene is associated with a rare form of epilepsy called familial focal epilepsy with variable foci (FFEVF). This type of epilepsy is characterized by seizures that originate in specific areas of the brain and can vary in location and severity.

NGS genetic testing is a type of genetic testing that uses next-generation sequencing technology to analyze multiple genes at once. This type of testing can help identify mutations or variations in the DEPDC5 gene that may be causing FFEVF.

Genetic testing for FFEVF can help with diagnosis, genetic counseling, and management of the condition. It can also help identify family members who may be at risk of developing the condition and allow for early intervention and treatment.

Test Components

  • Price: AED 4400.0
  • 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

Before undergoing the DEPDC5 Gene Epilepsy familial focal with variable foci Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with DEPDC5 Gene Epilepsy familial focal with variable foci.

For more information or to schedule an appointment, please contact our genetics department.

Test Name DEPDC5 Gene Epilepsy familial focal with variable foci 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 DEPDC5 Gene Epilepsy, familial focal with variable foci NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DEPDC5 Gene Epilepsy, familial focal with variable foci
Test Details

The DEPDC5 gene is associated with a rare form of epilepsy called familial focal epilepsy with variable foci (FFEVF). This type of epilepsy is characterized by seizures that originate in specific areas of the brain and can vary in location and severity.

NGS genetic testing is a type of genetic testing that uses next-generation sequencing technology to analyze multiple genes at once. This type of testing can help identify mutations or variations in the DEPDC5 gene that may be causing FFEVF.

Genetic testing for FFEVF can help with diagnosis, genetic counseling, and management of the condition. It can also help identify family members who may be at risk of developing the condition and allow for early intervention and treatment.