Pediatric Genetic Testing: Phenylalanine Newborn Screen Test
Introduction to the Phenylalanine Newborn Screen Test
The Phenylalanine Newborn Screen Test is an essential screening tool designed to detect phenylketonuria (PKU) in newborns. PKU is a genetic disorder that results in the inability to metabolize phenylalanine, an amino acid, leading to severe neurological damage if not treated early. This test is critical for ensuring timely interventions that can significantly improve a child’s quality of life.
What the Test Measures
This test measures the levels of phenylalanine in a newborn’s blood, which is essential for diagnosing PKU and other inborn errors of metabolism. Early detection allows for immediate dietary adjustments to prevent the harmful effects of high phenylalanine levels.
Who Should Consider This Test?
All newborns should undergo the Phenylalanine Newborn Screen Test as part of routine screening. Parents with a family history of metabolic disorders or those who notice symptoms such as:
- Unusual lethargy
- Seizures
- Vomiting
should consult a healthcare provider for further evaluation and testing.
Benefits of Taking the Test
- Early detection of PKU and other metabolic conditions.
- Prevention of severe developmental issues through dietary management.
- Peace of mind for parents regarding their child’s health.
Understanding Your Results
Results from the Phenylalanine Newborn Screen Test are typically available the next day. A normal result indicates that phenylalanine levels are within the acceptable range, while elevated levels may require further testing and dietary intervention. Your pediatrician will provide guidance based on the results.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Pediatric Phenylalanine Newborn Screen Test | 585 KSh | 650 KSh |
Our Services
We have branches across major cities in Kenya and offer home sample collection services for your convenience. To book the Phenylalanine Newborn Screen Test, please call or WhatsApp us at +254711564616.
Test Details
- 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.
- Turnaround Time: Sample collected Monday through Friday by 9 am; report available the next day.
- Specialty: Pediatrician
- Department: Genetic
- Method: Fluoroimmunoassay
- Disease Type: Inborn errors of metabolism
Ensure your newborn’s health with the Phenylalanine Newborn Screen Test today!
