TFAP2A Gene Branchiooculofacial Syndrome NGS Genetic DNA Test
Introduction to the Test
The TFAP2A Gene Branchiooculofacial Syndrome NGS Genetic DNA Test is a crucial diagnostic tool designed to identify genetic mutations associated with the Branchiooculofacial syndrome, a condition characterized by distinctive facial features and developmental anomalies. This test employs Next-Generation Sequencing (NGS) technology to analyze the TFAP2A gene, providing insights into the genetic basis of this syndrome.
What the Test Measures
This genetic test specifically measures alterations in the TFAP2A gene, which are linked to the development of Branchiooculofacial syndrome. By detecting these mutations, healthcare providers can better understand the genetic factors contributing to a patient’s condition.
Who Should Consider This Test
Individuals or families with a history of Branchiooculofacial syndrome or symptoms such as:
- Distinctive facial features
- Hearing loss
- Branchial cleft anomalies
- Other dysmorphic features
are encouraged to consider this test. Additionally, those with a family history of genetic disorders may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions.
- Informed family planning and management decisions.
- Access to targeted therapies and interventions.
- Peace of mind through understanding genetic risks.
Understanding Your Results
Results from the TFAP2A Gene Branchiooculofacial Syndrome NGS Genetic DNA Test will be provided in a comprehensive report. A genetic counselor will assist in interpreting the results, explaining the implications for the patient and their family. It is important to discuss any findings with a healthcare professional to understand their significance fully.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| TFAP2A Gene Branchiooculofacial Syndrome NGS Genetic DNA Test | 400,000 | 560,000 |
How to Book the Test
To book the TFAP2A Gene Branchiooculofacial Syndrome NGS Genetic DNA Test, please contact us at +2348110567037. Our team is ready to assist you with scheduling and any questions you may have regarding the test and its process.
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 the TFAP2A Gene Branchiooculofacial syndrome.
For more information, feel free to reach out to us! Your health is our priority.
