Newborn Screening Panel Extended Test
Introduction to the Newborn Screening Panel Extended Test
The Newborn Screening Panel Extended Test is a vital diagnostic tool designed to detect various inborn errors of metabolism in newborns. Conducted shortly after birth, this test plays a significant role in identifying metabolic disorders that can lead to severe health complications if left untreated. Early detection through this test allows for timely medical intervention, ensuring that affected infants receive the necessary care to lead healthy lives.
What the Test Measures
This comprehensive test measures several critical components, including:
- Biotinidase
- Cystic Fibrosis
- G6PD (Glucose-6-Phosphate Dehydrogenase)
- Galactosemia
- 17-Hydroxyprogesterone
- TSH (Thyroid-Stimulating Hormone)
- Tandem Mass Spectrometry – 30 Disorders
Who Should Consider This Test
The Newborn Screening Panel Extended Test is recommended for all newborns, particularly those with a family history of metabolic disorders or symptoms such as:
- Unexplained poor feeding
- Excessive sleepiness
- Vomiting
- Jaundice
- Failure to thrive
Benefits of Taking the Test
Taking the Newborn Screening Panel Extended Test offers several benefits, including:
- Early detection of metabolic disorders, which can prevent severe health issues.
- Access to early intervention strategies that can significantly improve health outcomes.
- Peace of mind for parents knowing their child is screened for potential health risks.
Understanding Your Results
After the test is conducted, results will be available the next day. It is essential to discuss the results with a qualified healthcare provider who can explain the implications and recommend any necessary follow-up actions based on the findings.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Newborn Screening Panel Extended Test | 140,000 NGN | 240,000 NGN |
Book the Test
To ensure the best health outcomes for your newborn, book the Newborn Screening Panel Extended Test today! Call or WhatsApp us at +2348077798758 to schedule your appointment.
Test Details
Turnaround Time: Sample must be submitted on Monday, Wednesday, or Friday by 9 am; reports are available the next day.
Sample Type: 1 drop of heel prick blood on 3 spots of filter paper. Samples must be shipped refrigerated or frozen, accompanied by clinical details and drug history.
Specialty: Pediatrician
Department: Genetic
Method: TMS, Fluoroimmunoassay
Disease Type: Inborn errors of metabolism
