Newborn Screening Panel 5 Test: Comprehensive Genetic Screening for Your Baby’s Health
Introduction to Newborn Screening
The Newborn Screening Panel 5 Test represents a crucial advancement in pediatric healthcare, offering comprehensive genetic screening during the critical first days of life. This state-of-the-art panel is designed to detect potentially life-threatening metabolic disorders before symptoms appear, enabling early intervention and treatment that can prevent serious developmental delays and lifelong complications.
What Does the Newborn Screening Panel 5 Test Measure?
This comprehensive screening panel evaluates four essential biomarkers through advanced fluoroimmunoassay technology:
- TSH (Thyroid-Stimulating Hormone) – Screens for congenital hypothyroidism, a condition affecting thyroid function that can impact growth and brain development
- G-6PD (Glucose-6-Phosphate Dehydrogenase) – Detects enzyme deficiency that can cause hemolytic anemia when exposed to certain foods or medications
- Biotinidase – Identifies biotinidase deficiency, which affects the body’s ability to process biotin (vitamin B7) and can lead to neurological problems
- Phenylalanine – Screens for phenylketonuria (PKU), a metabolic disorder that prevents proper breakdown of phenylalanine and can cause intellectual disability
Who Should Consider This Test?
The Newborn Screening Panel 5 Test is recommended for all newborns within the first 24-48 hours of life. Early screening is particularly important for:
- All newborn infants regardless of family history
- Babies with family history of metabolic disorders
- Infants born to parents with known genetic conditions
- Newborns showing no apparent symptoms but at risk for silent metabolic conditions
Key Benefits of Newborn Screening
Early detection through comprehensive newborn screening provides numerous advantages:
- Prevention of Developmental Delays – Early intervention can prevent intellectual disability and neurological damage
- Life-Saving Treatment – Many conditions detected are treatable with dietary modifications or medication
- Cost-Effective Healthcare – Early detection reduces long-term healthcare costs associated with untreated conditions
- Peace of Mind – Provides reassurance to parents about their newborn’s health status
- Improved Quality of Life – Early treatment enables normal development and healthy growth
Understanding Your Test Results
Your newborn screening results will be carefully interpreted by our genetic specialists:
- Normal Results – Indicate that your baby shows no signs of the screened conditions at this time
- Borderline Results – May require follow-up testing to confirm or rule out potential conditions
- Abnormal Results – Will be immediately communicated to your pediatrician for prompt intervention and treatment planning
All abnormal results are reviewed by our board-certified genetic counselors who will provide comprehensive guidance and next steps.
Test Pricing and Availability
| Price Type | Amount (USD) |
|---|---|
| Discount Price | $30 |
| Regular Price | $32 |
Nationwide Testing Availability
We have testing facilities conveniently located across the United States, serving families in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our network ensures that every newborn has access to this critical screening regardless of location.
Book Your Newborn Screening Today
Don’t leave your newborn’s health to chance. The Newborn Screening Panel 5 Test provides essential information that can shape your child’s future health and development. Our experienced pediatric genetic specialists are ready to assist you with this vital screening.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your newborn’s screening appointment. Our team will guide you through the simple process and answer any questions you may have about this important health assessment for your baby.
