SMARCA2 Gene Nicolaides Baraitser Syndrome NGS Genetic DNA Test
Introduction
The SMARCA2 Gene Nicolaides Baraitser Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to detect mutations in the SMARCA2 gene, which are associated with Nicolaides Baraitser syndrome. This syndrome is characterized by a range of developmental and physical anomalies, and early identification through genetic testing is crucial for effective management and intervention.
What the Test Measures
This genetic test utilizes Next-Generation Sequencing (NGS) technology to identify specific mutations within the SMARCA2 gene. By analyzing the genetic code, healthcare providers can determine if a patient has inherited the genetic markers associated with Nicolaides Baraitser syndrome.
Who Should Consider This Test
Individuals who may benefit from this test include:
- Patients exhibiting symptoms of developmental delays or physical anomalies.
- Families with a history of Nicolaides Baraitser syndrome.
- Those with risk factors such as dysmorphology or unexplained medical conditions.
Benefits of Taking the Test
Undergoing the SMARCA2 Gene Nicolaides Baraitser Syndrome NGS Genetic DNA Test offers several advantages:
- Accurate identification of genetic mutations.
- Informed decision-making for treatment and management options.
- Genetic counseling for affected families.
- Early intervention strategies to improve patient outcomes.
Understanding Your Results
Once the test is completed, results will be provided with general guidance on interpretation. It is essential to consult with a healthcare provider or genetic counselor to fully understand the implications of the results and to discuss potential next steps.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SMARCA2 Gene Nicolaides Baraitser Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking Your Test
To schedule your SMARCA2 Gene Nicolaides Baraitser Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any inquiries and to facilitate your booking process.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or even a single drop of blood on an FTA card. Prior to testing, a clinical history review and a genetic counseling session are recommended to construct a pedigree chart of family members affected by the syndrome.
