TBC1D24 Gene Familial Infantile Myoclonic Epilepsy NGS Genetic DNA Test
Introduction
The TBC1D24 Gene Familial Infantile Myoclonic Epilepsy NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with familial infantile myoclonic epilepsy. This test utilizes Next-Generation Sequencing (NGS) technology to provide comprehensive insights into the genetic factors that may contribute to this neurological disorder. By understanding these genetic predispositions, healthcare providers can offer tailored management plans for affected individuals and their families.
What the Test Measures
This test specifically measures variations in the TBC1D24 gene, which has been linked to familial infantile myoclonic epilepsy. Through detailed genetic analysis, the test can detect mutations that may lead to this condition, enabling early diagnosis and intervention.
Who Should Consider This Test?
Individuals with a family history of infantile myoclonic epilepsy or those exhibiting symptoms such as:
- Seizures during infancy
- Myoclonic jerks
- Developmental delays
should consider undergoing this genetic test. Additionally, individuals with risk factors such as having relatives diagnosed with the condition may also benefit from testing.
Benefits of Taking the Test
- Early identification of genetic predisposition to epilepsy
- Informed decision-making regarding family planning
- Personalized management strategies for affected individuals
- Access to genetic counseling and support resources
Understanding Your Results
Results from the TBC1D24 Gene Familial Infantile Myoclonic Epilepsy NGS Genetic DNA Test will be interpreted by a qualified genetic counselor or neurologist. They will provide insights into the significance of any detected mutations and discuss potential implications for family members. This guidance is crucial for understanding the next steps in managing health and wellness.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
To take the first step towards understanding your genetic health, book the TBC1D24 Gene Familial Infantile Myoclonic Epilepsy NGS Genetic DNA Test today. For inquiries or to schedule your appointment, please call or WhatsApp us at +2348077798758. Our team is here to assist you with any questions and guide you through the testing process.
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 is required, along with a genetic counseling session to draw a pedigree chart of family members affected with TBC1D24 Gene Familial Infantile Myoclonic Epilepsy.
Specialty: Neurology | Department: Genetics | Method: NGS Technology | Disease Type: Neurological Disorders
