Sale!

CHD2 Gene Epileptic encephalopathy childhood-onset Genetic Test

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

-21%

The CHD2 gene epileptic encephalopathy childhood-onset genetic test is a specialized diagnostic tool designed to identify mutations in the CHD2 gene, which have been associated with the development of early-onset epileptic encephalopathy. This condition is characterized by frequent seizures and significant neurodevelopmental delays occurring in childhood. The CHD2 gene plays a crucial role in brain development and function, and mutations in this gene can lead to various neurological issues, including epilepsy.

Conducted at DNA Labs UAE, this test provides a comprehensive analysis of the CHD2 gene to detect any genetic abnormalities that may contribute to the condition. By identifying specific mutations, the test can offer valuable information for the diagnosis, treatment planning, and management of affected individuals. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory using advanced genetic sequencing techniques.

The cost of the CHD2 gene epileptic encephalopathy childhood-onset genetic test at DNA Labs UAE is 4400 AED. This investment in testing can be crucial for families seeking answers to their child’s developmental and epileptic challenges, enabling them to access targeted therapies and interventions that can significantly improve the quality of life for those affected by this condition.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

CHD2 Gene Epileptic Encephalopathy Childhood-Onset Genetic Test

At DNA Labs UAE, we offer the CHD2 gene epileptic encephalopathy childhood-onset genetic test. This test is designed to diagnose and manage a rare genetic condition called epileptic encephalopathy, childhood-onset, which is associated with the CHD2 gene.

Test Components

The CHD2 gene epileptic encephalopathy childhood-onset genetic test includes the following 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 undergoing the CHD2 gene epileptic encephalopathy childhood-onset genetic test, it is important to provide the following information:

  • Clinical History of Patient who is going for CHD2 Gene Epileptic Encephalopathy, Childhood-Onset NGS Genetic DNA Test
  • A Genetic Counselling session to draw a pedigree chart of family members affected with CHD2 Gene Epileptic Encephalopathy, Childhood-Onset

Test Details

The CHD2 gene is associated with a rare genetic condition called epileptic encephalopathy, childhood-onset. This condition is characterized by the onset of seizures and developmental delay during early childhood. Seizures are often difficult to control with medication and can be accompanied by other neurological symptoms, such as intellectual disability and movement disorders.

NGS (next-generation sequencing) genetic testing is a type of DNA sequencing that can rapidly and accurately analyze multiple genes at once. The CHD2 gene NGS genetic test can detect mutations or variations in the CHD2 gene that may be responsible for epileptic encephalopathy, childhood-onset.

Genetic testing can be useful in diagnosing and managing this condition, as well as providing information about the risk of passing it on to future generations. It may also help guide treatment decisions and provide insight into potential comorbidities or complications.

It is important to note that genetic testing is not a substitute for clinical evaluation and diagnosis by a healthcare professional. If you or your child are experiencing seizures or other neurological symptoms, it is important to seek medical attention and evaluation.

Test Name CHD2 Gene Epileptic encephalopathy childhood-onset 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 CHD2 Gene Epileptic encephalopathy, childhood-onset NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CHD2 Gene Epileptic encephalopathy, childhood-onset
Test Details

The CHD2 gene is associated with a rare genetic condition called epileptic encephalopathy, childhood-onset. This condition is characterized by the onset of seizures and developmental delay during early childhood. The seizures are often difficult to control with medication and can be accompanied by other neurological symptoms, such as intellectual disability and movement disorders.

NGS (next-generation sequencing) genetic testing is a type of DNA sequencing that can rapidly and accurately analyze multiple genes at once. A CHD2 gene NGS genetic test can detect mutations or variations in the CHD2 gene that may be responsible for epileptic encephalopathy, childhood-onset.

Genetic testing can be useful in diagnosing and managing this condition, as well as providing information about the risk of passing it on to future generations. It may also help guide treatment decisions and provide insight into potential comorbidities or complications.

It is important to note that genetic testing is not a substitute for clinical evaluation and diagnosis by a healthcare professional. If you or your child are experiencing seizures or other neurological symptoms, it is important to seek medical attention and evaluation.