Fgf12 Gene Early Infantile Epileptic Encephalopathy Type 47 NGS Genetic DNA Test
Introduction
The Fgf12 Gene Early Infantile Epileptic Encephalopathy Type 47 NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify genetic mutations associated with severe neurological disorders in infants. Early diagnosis is crucial as it allows for timely interventions that can significantly improve the quality of life for affected children.
What the Test Measures
This genetic test specifically measures mutations in the FGF12 gene, which have been linked to early infantile epileptic encephalopathy type 47. By utilizing Next Generation Sequencing (NGS) technology, the test provides comprehensive insights into the genetic factors contributing to neurological disorders.
Who Should Consider This Test
Parents and caregivers should consider this test if their child exhibits symptoms such as:
- Severe seizures
- Developmental delays
- Unexplained neurological symptoms
Additionally, families with a history of neurological disorders may also benefit from this test to understand potential genetic risks.
Benefits of Taking the Test
- Early identification of genetic causes of neurological conditions.
- Informed decision-making regarding treatment options.
- Access to genetic counseling for affected families.
- Improved management and support strategies for affected children.
Understanding Your Results
Results from the Fgf12 Gene Early Infantile Epileptic Encephalopathy Type 47 NGS Genetic DNA Test typically take 3 to 4 weeks. A genetic counselor will help interpret the results, explaining the implications and potential next steps for your child’s health.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
Fgf12 Gene Early Infantile Epileptic Encephalopathy Type 47 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the Fgf12 Gene Early Infantile Epileptic Encephalopathy Type 47 NGS Genetic DNA Test or for more information, please call or WhatsApp us at +2348077798758. Ensure your child’s health is prioritized with timely and accurate genetic testing.