Newborn Screening Panel 2 Test
Introduction to the Newborn Screening Panel 2 Test
The Newborn Screening Panel 2 Test is a vital diagnostic tool designed to identify inborn errors of metabolism in newborns. Early detection of these metabolic disorders can significantly improve health outcomes for infants, allowing for timely interventions and management strategies. This test is crucial for pediatricians and families to ensure that any potential health issues are addressed promptly.
What the Test Measures/Detects
This test specifically measures the levels of Thyroid-Stimulating Hormone (TSH) and Glucose-6-Phosphate Dehydrogenase (G-6PD) in a small sample of blood. High or low levels of these substances can indicate serious metabolic conditions that require immediate attention.
Who Should Consider This Test
All newborns should undergo the Newborn Screening Panel 2 Test, especially those with:
- A family history of metabolic disorders
- Symptoms such as jaundice, lethargy, or feeding difficulties
- Risk factors associated with metabolic diseases
This test is a standard procedure in many healthcare settings to ensure the health and well-being of infants.
Benefits of Taking the Test
- Early detection of metabolic disorders
- Timely intervention can prevent severe health complications
- Peace of mind for parents regarding their child’s health
- Guidance for pediatricians in managing potential health issues
Understanding Your Results
Results from the Newborn Screening Panel 2 Test are typically available the next day, providing quick insights into your child’s metabolic health. If results indicate abnormalities, your pediatrician will discuss further testing and treatment options.
Test Name and Price
| Discount Price | Regular Price |
|---|---|
| 11,700 NGN | 13,000 NGN |
How to Book the Test
To ensure your newborn receives the best care, book the Newborn Screening Panel 2 Test today! Contact us at +2348110567037 or visit our website to schedule your appointment.
Additional Information
Turnaround Time: Sample must be submitted Monday through Friday by 9 am; reports are available the next day.
Sample Type: 1 drop of heel prick blood on 3 spots of filter paper, available from LPL. Samples should be shipped refrigerated or frozen, and clinical details along with drug history must accompany the sample.
Test Components: TSH, G-6PD
Pre-Test Instructions: Clinical details and drug history must accompany the sample.
Specialty: Pediatrician
Department: Genetic
Method: Fluoroimmunoassay
Disease Type: Inborn Errors of Metabolism
