ACTG1 Gene Baraitser-Winter Syndrome Type 2 NGS Genetic DNA Test
Introduction to the ACTG1 Gene Baraitser-Winter Syndrome Type 2 NGS Genetic DNA Test
The ACTG1 Gene Baraitser-Winter Syndrome Type 2 NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the ACTG1 gene. This test is crucial for diagnosing Baraitser-Winter syndrome type 2, a condition characterized by distinct physical features and developmental challenges.
What the Test Measures
This genetic test specifically measures the presence of mutations in the ACTG1 gene, which are linked to Baraitser-Winter syndrome type 2. By analyzing the genetic material obtained from a blood sample, healthcare providers can determine if an individual has inherited this condition.
Who Should Consider This Test
Individuals who may benefit from the ACTG1 Gene Baraitser-Winter Syndrome Type 2 NGS Genetic DNA Test include:
- Patients exhibiting symptoms of dysmorphology.
- Individuals with a family history of Baraitser-Winter syndrome.
- Parents seeking to understand genetic risks for their children.
Benefits of Taking the Test
- Accurate diagnosis of Baraitser-Winter syndrome type 2.
- Informed family planning decisions based on genetic insights.
- Access to targeted treatments and interventions.
- Enhanced understanding of the condition for better management.
Understanding Your Results
Once the test is completed, results will indicate whether a mutation in the ACTG1 gene is present. A genetic counseling session will help interpret the results and discuss potential implications for the patient and their family.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
Don’t wait to gain valuable insights into your genetic health. Book the ACTG1 Gene Baraitser-Winter Syndrome Type 2 NGS Genetic DNA Test today by calling or WhatsApping us at +2348110567037.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. Please ensure to provide a clinical history and consider a genetic counseling session to draw a pedigree chart of family members affected by ACTG1 Gene Baraitser-Winter syndrome type 2.
