Newborn Screening Panel 7 Test
Introduction to the Newborn Screening Panel 7 Test
The Newborn Screening Panel 7 Test is a crucial diagnostic assessment performed shortly after birth to detect various inborn errors of metabolism. Early detection of these conditions can significantly improve health outcomes for newborns. This test is essential for pediatricians and parents who want to ensure their child’s healthy development from the start.
What the Test Measures
This comprehensive test measures the following components:
- G6PD (Glucose-6-Phosphate Dehydrogenase) Deficiency
- TSH (Thyroid-Stimulating Hormone) Levels
- Phenylalanine Levels
- Cystic Fibrosis
- 17-Hydroxyprogesterone Levels
- Galactosemia
- Biotinidase Deficiency
Who Should Consider This Test?
All newborns should undergo the Newborn Screening Panel 7 Test, especially if there are risk factors such as:
- Family history of metabolic disorders
- Symptoms of metabolic issues (e.g., poor feeding, lethargy)
Benefits of Taking the Test
Taking the Newborn Screening Panel 7 Test has several benefits:
- Early detection of metabolic disorders, allowing for timely intervention.
- Prevention of severe health complications associated with untreated conditions.
- Peace of mind for parents regarding their child’s health.
Understanding Your Results
After the test is conducted, results will be available the next day. It is essential to discuss these results with your pediatrician, who can provide guidance on any necessary follow-up actions or treatments based on the findings.
Test Pricing
Discount Price | 60,000 NGN |
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Regular Price | 90,000 NGN |
Book Your Test Today!
To ensure the best start for your newborn, book the Newborn Screening Panel 7 Test today. Call or WhatsApp us at +2348077798758 to schedule your appointment. Remember, early detection is key to a healthy future!
Test Details
Turnaround Time: Sample must be submitted Monday through Friday by 9 AM; report available 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: Clinical details and drug history must accompany the sample.
Specialty: Pediatrician
Department: Genetic
Method: Fluoroimmunoassay
Disease Type: Inborn errors of metabolism