TTC21B Gene Nephronophthisis Type 12 NGS Genetic DNA Test
Introduction
The TTC21B Gene Nephronophthisis Type 12 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with nephronophthisis, a rare kidney disorder. This test employs Next-Generation Sequencing (NGS) technology to provide precise genetic insights, which are essential for effective patient management and treatment planning.
What the Test Measures
This genetic test specifically measures alterations in the TTC21B gene, which plays a crucial role in kidney function and development. By analyzing the DNA, healthcare providers can determine if a patient carries mutations that may lead to nephronophthisis or other related disorders.
Who Should Consider This Test?
Individuals who may benefit from the TTC21B Gene Nephronophthisis Type 12 NGS Genetic DNA Test include:
- Patients with a family history of nephronophthisis.
- Individuals exhibiting symptoms such as kidney dysfunction or renal failure.
- Those with a genetic predisposition to kidney disorders.
Benefits of Taking the Test
Taking the TTC21B Gene Nephronophthisis Type 12 NGS Genetic DNA Test offers several advantages:
- Accurate diagnosis of genetic conditions.
- Informed decision-making regarding treatment options.
- Family planning insights for at-risk individuals.
- Access to specialized medical care tailored to genetic findings.
Understanding Your Results
Results from the TTC21B Gene Nephronophthisis Type 12 NGS Genetic DNA Test will be interpreted by qualified genetic counselors and medical professionals. They will provide guidance on the implications of the findings, potential health risks, and the next steps in management.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| TTC21B Gene Nephronophthisis Type 12 NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Book the Test
To take the TTC21B Gene Nephronophthisis Type 12 NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website to book your appointment. Ensure you have a clinical history ready and consider a genetic counseling session to discuss your family’s health background.
Turnaround time for results is approximately 3 to 4 weeks. The sample type required can be blood, extracted DNA, or one drop of blood on an FTA card. Take the first step towards understanding your genetic health today!
