KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 NGS Genetic DNA Test
Introduction
The KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 NGS Genetic DNA Test is a vital diagnostic tool designed to identify genetic mutations associated with severe neurological disorders in infants. This test employs Next-Generation Sequencing (NGS) technology to analyze the KCNA2 gene, which plays a crucial role in the proper functioning of neurons. Early detection of mutations can significantly impact treatment options and outcomes for affected children.
What the Test Measures
This genetic test specifically detects mutations in the KCNA2 gene, which are linked to early infantile epileptic encephalopathy type 32. By identifying these mutations, healthcare providers can diagnose the condition more accurately, allowing for timely intervention.
Who Should Consider This Test
Parents should consider the KCNA2 Gene test if their child exhibits:
- Severe seizures that are difficult to control
- Developmental delays or regression
- Abnormal neurological examination findings
Additionally, a family history of similar neurological disorders may warrant testing.
Benefits of Taking the Test
- Accurate diagnosis of KCNA2 gene mutations
- Informed treatment decisions based on genetic findings
- Better understanding of the condition and its implications for family members
- Access to genetic counseling services for affected families
Understanding Your Results
Results from the KCNA2 Gene test can provide crucial information regarding the presence of mutations. A genetic counselor will help you interpret the results and discuss potential implications for your child’s health and future.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for the test can be blood, extracted DNA, or one drop of blood on an FTA card.
Before the test, it is essential to provide a clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected by similar conditions.
Book Your Test Today!
We have branches across Kenya and offer a convenient home sample collection service. For more information or to book the KCNA2 Gene Early Infantile Epileptic Encephalopathy Type 32 NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
