NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test
Introduction
The NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to analyze the NR2E1 gene. This gene has been associated with polymicrogyria, a neurological disorder characterized by abnormal brain development. Understanding the genetic basis of this condition is crucial for early diagnosis and effective management.
What the Test Measures
This genetic test specifically detects variations in the NR2E1 gene that may contribute to the development of bilateral occipital polymicrogyria. By examining these genetic markers, healthcare providers can better understand the risk of neurological disorders in patients.
Who Should Consider This Test
This test is recommended for individuals who exhibit symptoms of neurological disorders or have a family history of conditions linked to the NR2E1 gene. Symptoms may include developmental delays, seizures, and cognitive impairments. Additionally, individuals undergoing genetic counseling may find this test beneficial for assessing risk factors.
Benefits of Taking the Test
- Early diagnosis of potential neurological disorders.
- Guidance for treatment options based on genetic predispositions.
- Informed family planning through understanding genetic risks.
- Access to specialized care from neurologists and geneticists.
Understanding Your Results
Results from the NR2E1 Gene Polymicrogyria test will provide insights into the presence of genetic mutations associated with the disorder. A genetic counseling session is recommended to help interpret the results and discuss the implications for you and your family.
Test Pricing
| Discount Price | 400000 NGN |
|---|---|
| Regular Price | 560000 NGN |
Book the Test
Ready to take the next step? Book your NR2E1 Gene Polymicrogyria Bilateral Occipital NGS Genetic DNA Test today! For inquiries or to schedule your appointment, please call or WhatsApp us at +2348077798758.
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 by NR2E1 Gene Polymicrogyria.
Consult with a neurologist or geneticist to understand the implications of this test and how it can assist in managing neurological disorders.
