Newborn Screening Panel 4 Test
Introduction to the Newborn Screening Panel 4 Test
The Newborn Screening Panel 4 Test is a crucial diagnostic examination designed to identify specific metabolic disorders in newborns. Early detection of these conditions can significantly improve health outcomes and prevent serious complications. This test is particularly important as it screens for disorders that may not present immediate symptoms but can lead to severe health issues if left undiagnosed.
What the Test Measures
This test measures the levels of several key components that are indicative of metabolic disorders:
- Thyroid Stimulating Hormone (TSH)
- Glucose-6-Phosphate Dehydrogenase (G-6PD)
- 17-Hydroxyprogesterone
- Total Galactose
Who Should Consider This Test?
All newborns should undergo the Newborn Screening Panel 4 Test, especially those with a family history of metabolic disorders or who exhibit symptoms such as:
- Unexplained jaundice
- Failure to thrive
- Abnormal feeding patterns
Early testing is vital for timely intervention and management of any detected conditions.
Benefits of Taking the Test
Taking the Newborn Screening Panel 4 Test offers numerous benefits, including:
- Early detection of potentially life-threatening metabolic disorders.
- Access to prompt treatment and management options.
- Peace of mind for parents regarding their child’s health.
- Improved long-term health outcomes for affected newborns.
Understanding Your Results
Results from the Newborn Screening Panel 4 Test will be available the next day. If any abnormalities are detected, our pediatric specialists will provide guidance and discuss the next steps for further evaluation and management. It is essential to understand that not all positive results indicate a disorder; further testing may be required.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Newborn Screening Panel 4 Test | 23,400 | 26,000 |
Booking the Test
To ensure your newborn receives this essential screening, contact us today to book the Newborn Screening Panel 4 Test. Call or WhatsApp us at +2348077798758. Don’t wait—early detection can make all the difference in your child’s health!
Turnaround Time: Sample collection must be done Monday through Friday by 9 AM; reports will be available the next day.
Sample Type: 1 drop of heel prick blood each on 3 spots of filter paper available from LPL. Ship refrigerated or frozen. Clinical details and drug history must accompany the sample.
Pre-Test Instructions: Ensure clinical details and drug history accompany the sample.
Specialty: Pediatrician | Department: Genetic | Method: Fluoroimmunoassay | Disease Type: Inborn Errors of Metabolism
