ZEB2 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test
Introduction
The ZEB2 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify mutations in the ZEB2 gene. This gene is crucial for the proper functioning of the respiratory system, and its mutations can lead to severe respiratory issues, particularly in infants and children. Early detection through this test can significantly improve patient outcomes and management strategies.
What the Test Measures
This genetic test specifically measures the presence of mutations in the ZEB2 gene, which are linked to congenital central hypoventilation syndrome (CCHS). By analyzing the patient’s DNA, healthcare providers can determine if there are any genetic predispositions that may affect respiratory function.
Who Should Consider This Test?
Patients who exhibit symptoms such as:
- Severe respiratory difficulties, particularly during sleep
- History of unexplained hypoxia
- Family history of central hypoventilation syndrome
Additionally, individuals with risk factors such as a known family history of ZEB2 mutations should consider this test for proactive management.
Benefits of Taking the Test
- Early diagnosis and intervention for respiratory issues.
- Informed decision-making regarding patient care and management.
- Potential for targeted therapies and personalized treatment plans.
- Genetic counseling for family members to assess risk.
Understanding Your Results
Results from the ZEB2 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test will indicate whether mutations are present. A genetic counselor will help interpret the results, providing guidance on management and potential implications for family members.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| ZEB2 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Test Details
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 by the ZEB2 gene.
Book Your Test Today!
We have branches across all major cities in Kenya, providing convenient access to our services. To book the ZEB2 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test or for more information, please call or WhatsApp us at +254711564616.
