Newborn Screening Panel 5 Test
Introduction to the Newborn Screening Panel 5 Test
The Newborn Screening Panel 5 Test is a vital assessment performed on newborns to detect certain metabolic disorders that can lead to severe health issues if not identified and treated early. This test is essential for ensuring the health and well-being of infants, allowing for timely medical interventions that can significantly improve outcomes.
What the Test Measures
This comprehensive screening evaluates five critical metabolic components:
- TSH (Thyroid-Stimulating Hormone)
- G-6PD (Glucose-6-Phosphate Dehydrogenase)
- Biotinidase
- Phenylalanine
These components are essential for the body’s metabolic processes, and their deficiencies can lead to serious health issues if not addressed promptly.
Who Should Consider This Test?
All newborns should undergo the Newborn Screening Panel 5 Test as a standard practice, especially those with:
- Family history of metabolic disorders
- Symptoms like jaundice, poor feeding, or lethargy
- Any known risk factors for inborn errors of metabolism
Benefits of Taking the Test
- Early detection of metabolic disorders, allowing for prompt treatment.
- Prevention of serious complications associated with untreated conditions.
- Peace of mind for parents regarding their newborn’s health.
- Facilitates informed decision-making for ongoing care and management.
Understanding Your Results
Results from the Newborn Screening Panel 5 Test are typically available the next day. It is essential to consult with a pediatrician or healthcare provider to interpret the results accurately. Positive results may require further testing or immediate intervention, while negative results generally indicate normal metabolic function.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 23,400 NGN |
| Regular Price | 26,000 NGN |
Book the Test Today!
Don’t wait to ensure your newborn’s health. Book the Newborn Screening Panel 5 Test today by calling or sending a WhatsApp message to +2348077798758. Ensure your baby has the best start in life!
For sample collection, a drop of heel prick blood is required on three spots of filter paper. Please ensure clinical details and drug history accompany the sample. Samples should be shipped refrigerated or frozen.
This test is performed by expert pediatricians in our Genetic department using advanced Fluoroimmunoassay methods to detect inborn errors of metabolism effectively.
