NODAL Gene Heterotaxy Visceral Type 5 NGS Genetic DNA Test
Introduction to the NODAL Gene Heterotaxy Test
The NODAL Gene Heterotaxy Visceral Type 5 NGS Genetic DNA Test is an advanced diagnostic tool designed to assess genetic variations associated with heterotaxy, a condition where internal organs are arranged abnormally. This test is particularly relevant for pediatric patients with congenital heart defects and other associated anomalies.
What the Test Measures
This genetic test employs Next-Generation Sequencing (NGS) technology to detect mutations in the NODAL gene. By analyzing the genetic material, the test can identify specific mutations that may lead to visceral organ malformations.
Who Should Consider This Test?
Individuals who should consider this test include:
- Children diagnosed with congenital heart defects.
- Patients with a family history of heterotaxy or related genetic conditions.
- Individuals exhibiting symptoms such as abnormal organ placement or unexplained congenital anomalies.
Benefits of Taking the Test
The benefits of the NODAL Gene Heterotaxy Visceral Type 5 NGS Genetic DNA Test include:
- Accurate identification of genetic mutations that may affect treatment options.
- Facilitating early intervention and management of associated health issues.
- Providing valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the NODAL Gene Heterotaxy test will provide insights into the genetic factors contributing to the patient’s condition. It is essential to discuss the results with a qualified genetic counselor or healthcare provider to understand their implications fully.
Test Details and Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
NODAL Gene Heterotaxy Visceral Type 5 NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Booking Your Test
To book the NODAL Gene Heterotaxy Visceral Type 5 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with the booking process and any inquiries you may have.
Test Parameters
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected.
Ensure you consult with your healthcare provider before taking the test for the best outcomes.