Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test
Introduction to the Test
The Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify genetic mutations associated with Primary Ciliary Dyskinesia (PCD). PCD is a genetic disorder affecting the cilia, the tiny hair-like structures that line the respiratory tract and other organs, leading to chronic respiratory problems and other complications. Understanding your genetic predisposition can significantly impact your treatment options and management strategies.
What the Test Measures
This genetic test specifically analyzes the Spag1 gene to detect mutations that may lead to Primary Ciliary Dyskinesia. By identifying these mutations, healthcare providers can better understand the underlying causes of symptoms and tailor treatment plans accordingly.
Who Should Consider This Test?
This test is recommended for individuals exhibiting symptoms of PCD, such as:
- Chronic respiratory infections
- Persistent cough
- Difficulty breathing
- Ear infections
- Infertility issues
Additionally, those with a family history of genetic disorders or symptoms consistent with PCD should consider undergoing this test.
Benefits of Taking the Test
Taking the Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test offers several benefits:
- Accurate diagnosis of genetic causes of respiratory issues
- Informed decision-making regarding treatment options
- Family planning and genetic counseling for potential hereditary conditions
- Better management of symptoms and overall health
Understanding Your Results
Results from the Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test will be provided in detail, explaining any detected mutations and their implications. It is essential to discuss these results with your healthcare provider to understand their significance and the next steps in your care plan.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
Ready to take the next step in understanding your health? Book the Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test today! For appointments, please call or WhatsApp us at +2348077798758.
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 with the SLC52A3 Gene Brown-Vialetto-Van Laere syndrome.
Consult with an ENT Doctor or a specialist in Genetics for further guidance and support.
