Hydin Gene Primary Ciliary Dyskinesia Type 5 NGS Genetic DNA Test
Introduction
The Hydin Gene Primary Ciliary Dyskinesia Type 5 NGS Genetic DNA Test is an advanced diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to analyze the Hydin gene associated with primary ciliary dyskinesia (PCD). PCD is a genetic disorder that affects the cilia, leading to respiratory and fertility issues. Understanding your genetic predisposition to this condition is crucial for early diagnosis and management.
What the Test Measures
This test specifically measures mutations in the Hydin gene, which are known to disrupt normal ciliary function. By identifying these mutations, healthcare providers can better understand the underlying causes of respiratory issues in patients.
Who Should Consider This Test?
Individuals experiencing chronic respiratory problems, recurrent ear infections, or other symptoms associated with ciliary dysfunction should consider this test. Additionally, those with a family history of PCD or related disorders may benefit from genetic testing to assess their risk factors.
Benefits of Taking the Test
- Early diagnosis of primary ciliary dyskinesia.
- Informed management and treatment options tailored to individual genetic profiles.
- Peace of mind for patients and families regarding hereditary conditions.
Understanding Your Results
Results from the Hydin Gene Primary Ciliary Dyskinesia Type 5 NGS Genetic DNA Test will provide insight into the presence of mutations. A genetic counselor will help interpret these results, guiding you on the next steps based on your genetic profile.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Hydin Gene Primary Ciliary Dyskinesia Type 5 NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
How to Book the Test
To schedule your Hydin Gene Primary Ciliary Dyskinesia Type 5 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any inquiries and guide you through the booking process.
Additional Information
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 Patient who is going for PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN40
Specialty: ENT Doctor
Department: Genetics
Method: NGS Technology
Disease Type: Ear Nose Throat Disorders
