XRCC4 Gene Short Stature Microcephaly and Endocrine Dysfunction NGS Genetic DNA Test
Introduction
The XRCC4 Gene Short Stature Microcephaly and Endocrine Dysfunction NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic abnormalities associated with short stature, microcephaly, and various endocrine dysfunctions. This test utilizes Next Generation Sequencing (NGS) technology, providing precise insights into the genetic factors that may contribute to these conditions. Understanding these genetic links is crucial for effective management and treatment strategies.
What the Test Measures
This genetic test specifically measures variations in the XRCC4 gene, which is known to play a significant role in DNA repair and cellular function. By analyzing the genetic sequence, the test can detect mutations that may lead to the aforementioned health issues.
Who Should Consider This Test?
Individuals who exhibit symptoms such as:
- Short stature
- Microcephaly (abnormally small head size)
- Endocrine dysfunctions (hormonal imbalances)
Additionally, families with a history of these conditions may benefit from this test to better understand their genetic risks.
Benefits of Taking the Test
- Accurate identification of genetic conditions.
- Informed decision-making regarding treatment options.
- Guidance for family planning and genetic counseling.
- Improved understanding of the patient’s health and potential risks.
Understanding Your Results
Upon completion of the test, patients will receive a detailed report outlining the findings. It is essential to consult with a healthcare professional to interpret the results accurately and discuss potential next steps.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Booking the Test
To book the XRCC4 Gene Short Stature Microcephaly and Endocrine Dysfunction NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling and any inquiries you may have.
Additional Information
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.
For more information, feel free to reach out to our support team or visit our website.
