PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Genetic DNA Test
Introduction
The PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Genetic DNA Test is a specialized genetic test that plays a vital role in diagnosing Auriculocondylar Syndrome, a condition characterized by specific facial abnormalities and ear anomalies. By utilizing Next Generation Sequencing (NGS) technology, this test provides a comprehensive analysis of the PLCB4 gene, which is crucial for understanding the genetic basis of this syndrome.
What the Test Measures
This test measures the presence of mutations in the PLCB4 gene, which are known to be associated with Auriculocondylar Syndrome Type 2. It detects changes at the DNA level that may lead to the development of this syndrome, helping healthcare providers make informed decisions regarding diagnosis and management.
Who Should Consider This Test
This test is recommended for individuals who exhibit symptoms of dysmorphology, particularly those with facial anomalies or ear deformities. Additionally, family members of diagnosed individuals may also consider testing to understand their genetic risk and implications.
Benefits of Taking the Test
- Provides clarity on genetic predispositions associated with Auriculocondylar Syndrome.
- Guides treatment options and management strategies for affected individuals.
- Offers valuable information for family planning and genetic counseling.
- Helps in understanding the inheritance patterns of the condition.
Understanding Your Results
Results from the PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Genetic DNA Test will typically be available within 3 to 4 weeks. A genetic counselor will help interpret the results and discuss their implications, ensuring you understand the outcomes and next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
How to Book the Test
To book the PLCB4 Gene Auriculocondylar Syndrome Type 2 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any inquiries you may have.
Sample Type and Pre-Test Instructions
The sample required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to testing, a clinical history of the patient is essential, along with a genetic counseling session to draw a pedigree chart of family members affected by the PLCB4 gene.
