KMT2A Gene Wiedemann-Steiner Syndrome NGS Genetic DNA Test
Introduction
The KMT2A Gene Wiedemann-Steiner Syndrome NGS Genetic DNA Test is a state-of-the-art diagnostic tool that plays a vital role in identifying genetic mutations linked to Wiedemann-Steiner syndrome. This genetic condition is characterized by a range of developmental and physical anomalies, and early detection is crucial for effective management and treatment.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to detect mutations in the KMT2A gene, which are associated with Wiedemann-Steiner syndrome. By analyzing the genetic material from a blood sample or extracted DNA, the test provides insights into the presence of these mutations.
Who Should Consider This Test
Individuals who exhibit symptoms of Wiedemann-Steiner syndrome or those with a family history of the condition should consider this test. Common symptoms include:
- Developmental delays
- Distinctive facial features
- Growth abnormalities
If you or your family members show any of these symptoms, consulting with a healthcare provider about this test may be beneficial.
Benefits of Taking the Test
The KMT2A Gene Wiedemann-Steiner Syndrome NGS Genetic DNA Test offers several advantages:
- Accurate identification of genetic mutations
- Informed decision-making for treatment and management
- Insight into familial risk factors
- Guidance for genetic counseling and support
Understanding Your Results
Once the test is completed, results will be provided to you along with general guidance on interpretation. It is important to discuss these results with a healthcare professional who can provide clarity and advice on next steps.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| KMT2A Gene Wiedemann-Steiner Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the KMT2A Gene Wiedemann-Steiner Syndrome NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your appointment and answering any questions you may have.
Turnaround time for results is approximately 3 to 4 weeks. Pre-test instructions include providing a clinical history and undergoing a genetic counseling session to create a pedigree chart of affected family members.
Sample types accepted include blood, extracted DNA, or one drop of blood on an FTA card.
