LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles LAMC1 Related NGS Genetic DNA Test
Introduction
The LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test is a specialized genetic test designed to detect mutations in the LAMC1 gene, which are associated with Dandy-Walker malformation and occipital cephaloceles. These conditions are types of brain malformations that can lead to significant neurological issues. Understanding the genetic basis of these conditions is crucial for early diagnosis and effective management.
What the Test Measures
This test specifically measures the presence of mutations in the LAMC1 gene. By analyzing the genetic material from a blood or DNA sample, the test can identify whether an individual is a carrier of the mutation associated with these malformations.
Who Should Consider This Test
Individuals or families with a history of Dandy-Walker malformation or occipital cephaloceles should consider this test. Symptoms may include developmental delays, coordination issues, and other neurological concerns. Risk factors include a family history of these conditions and the presence of related symptoms in newborns or young children.
Benefits of Taking the Test
- Early diagnosis allows for better management and treatment options.
- Informed family planning can be achieved through understanding genetic risks.
- Access to genetic counseling for affected families.
- Peace of mind for individuals and families regarding their health.
Understanding Your Results
Results from the LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test will provide insights into the presence or absence of the LAMC1 gene mutation. A genetic counselor will help interpret the results and discuss potential implications for the patient and their family.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 400000 NGN | 560000 NGN |
Booking the Test
To schedule your LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any questions you may have and guide you through the booking 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 and a genetic counseling session to draw a pedigree chart of family members affected with the LAMC1 gene is required.
This test falls under the Pediatrics specialty, within the Genetics department, utilizing NGS Technology to assess dysmorphology-related conditions.
