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CUX2 Gene Early infantile epileptic encephalopathy type 67 Genetic Test

4,400 د.إ

-21%

The CUX2 gene is implicated in early infantile epileptic encephalopathy type 67 (EIEE67), a severe form of epilepsy that manifests in infancy. This condition is characterized by frequent seizures and significant developmental delays, impacting the quality of life of affected individuals. Genetic testing for mutations in the CUX2 gene is crucial for the accurate diagnosis of EIEE67, enabling appropriate management and treatment strategies.

DNA Labs UAE offers a specialized genetic test for the CUX2 gene to identify mutations associated with early infantile epileptic encephalopathy type 67. The test is priced at 4400 AED and is conducted in a state-of-the-art laboratory setting by professionals who specialize in genetic diagnostics. This test is essential for families seeking answers to unexplained seizures in infants, providing them with critical information for medical decision-making and potential therapeutic interventions.

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CUX2 Gene Early infantile epileptic encephalopathy type 67 Genetic Test

Are you concerned about early infantile epileptic encephalopathy type 67 (EIEE67)? DNA Labs UAE offers the CUX2 Gene Early infantile epileptic encephalopathy type 67 Genetic Test to help diagnose this rare genetic disorder.

Test Details

The CUX2 gene is associated with EIEE67, a condition that affects the brain and causes seizures. Symptoms of EIEE67 include the onset of seizures within the first few months of life, developmental delay, intellectual disability, and other neurological problems.

NGS Technology

Our CUX2 gene NGS genetic test utilizes next-generation sequencing (NGS) technology to analyze multiple genes simultaneously. This comprehensive analysis of a patient’s genetic makeup helps identify potential genetic causes of EIEE67.

Test Components

  • 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

Prior to the CUX2 gene NGS 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 EIEE67. This information aids in accurate diagnosis and treatment decisions.

Benefits of the Test

If a mutation or variation is identified in the CUX2 gene, it can help diagnose EIEE67 and guide treatment decisions. Furthermore, the test provides important information for genetic counseling and family planning.

Don’t wait any longer. Contact DNA Labs UAE today to schedule your CUX2 Gene Early infantile epileptic encephalopathy type 67 Genetic Test.

Test Name CUX2 Gene Early infantile epileptic encephalopathy type 67 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 CUX2 Gene Early infantile epileptic encephalopathy type 67 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CUX2 Gene Early infantile epileptic encephalopathy type 67
Test Details

The CUX2 gene is associated with early infantile epileptic encephalopathy type 67 (EIEE67), which is a rare genetic disorder that affects the brain and causes seizures. EIEE67 is characterized by the onset of seizures within the first few months of life, developmental delay, intellectual disability, and other neurological problems.

NGS genetic testing is a type of genetic testing that uses next-generation sequencing technology to analyze multiple genes simultaneously. This type of testing can provide a comprehensive analysis of a patient’s genetic makeup and identify potential genetic causes of a disease.

A CUX2 gene NGS genetic test would involve sequencing the entire CUX2 gene to look for any genetic mutations or variations that may be causing EIEE67. If a mutation is identified, it can help diagnose the condition and guide treatment decisions. It can also provide important information for genetic counseling and family planning.