PLCB1 Gene Early Infantile Epileptic Encephalopathy Type 12 NGS Genetic DNA Test
Introduction to the Test
The PLCB1 Gene Early Infantile Epileptic Encephalopathy Type 12 NGS Genetic DNA Test is designed to identify mutations in the PLCB1 gene that may lead to early infantile epileptic encephalopathy (EIEE). This neurological disorder is characterized by seizures that begin in infancy and can lead to significant developmental delays. Understanding the genetic basis of this condition is vital for appropriate management and treatment.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the PLCB1 gene. It detects specific mutations that are associated with EIEE, providing critical information for diagnosis and potential treatment options.
Who Should Consider This Test?
Parents or guardians should consider the PLCB1 Gene Early Infantile Epileptic Encephalopathy Type 12 NGS Genetic DNA Test if their child exhibits:
- Recurrent seizures starting in infancy
- Developmental delays
- Family history of epilepsy or neurological disorders
Benefits of Taking the Test
There are several benefits to taking this test:
- Early and accurate diagnosis of genetic causes of seizures
- Informed treatment planning and management
- Potential for genetic counseling for families
- Understanding the risk of recurrence in future pregnancies
Understanding Your Results
Results from the PLCB1 Gene test can help in understanding the specific genetic causes of your child’s condition. A healthcare provider will explain the findings and discuss potential treatment options based on the results.
Test Pricing
| Price Type | Price (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To book the PLCB1 Gene Early Infantile Epileptic Encephalopathy Type 12 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and any questions you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-test Instructions: A clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with PLCB1 Gene Early Infantile Epileptic Encephalopathy Type 12 is required.
This test is conducted by specialists in the field of genetics and neurology, ensuring high-quality results and expert guidance in managing neurological disorders.
