Newborn Screening Panel NBS Quad Test
Introduction to the Newborn Screening Panel NBS Quad Test
The Newborn Screening Panel NBS Quad Test is a vital screening tool for newborns, designed to detect serious metabolic disorders that can affect a child’s development and overall health. Early detection through this test enables timely intervention, which can significantly improve health outcomes and prevent long-term complications.
What the Test Measures
This comprehensive panel tests for four critical metabolic conditions:
- Thyroid-Stimulating Hormone (TSH)
- 17-Hydroxyprogesterone
- Phenylalanine
- Galactosemia
Who Should Consider This Test
All newborns should undergo the Newborn Screening Panel NBS Quad Test, especially those with:
- A family history of metabolic disorders
- Symptoms such as poor feeding, vomiting, or lethargy
- Risk factors associated with genetic conditions
Benefits of Taking the Test
- Early detection of serious health issues
- Timely intervention can prevent complications
- Peace of mind for parents regarding their child’s health
Understanding Your Results
Results from the Newborn Screening Panel NBS Quad Test will be available the next day after sample collection. A pediatrician will provide guidance on interpreting the results and discuss any necessary follow-up actions.
Test Information and Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
Newborn Screening Panel NBS Quad Test | 23,400 NGN | 26,000 NGN |
How to Book the Test
Booking the Newborn Screening Panel NBS Quad Test is simple. Contact us at DNA Labs Nigeria via phone or WhatsApp at +2348077798758 to schedule your appointment. Ensure your newborn’s health today!
Turnaround Time: Samples are accepted Monday through Friday by 9 AM, with reports available the next day.
Sample Type: A drop of heel prick blood on three spots of filter paper, which must be shipped refrigerated or frozen. Clinical details and drug history must accompany the sample.
Specialty: Pediatrician
Department: Genetic
Method: Fluoroimmunoassay
Disease Type: Inborn Errors of Metabolism