Newborn Screening Panel NBS Quad Test
Comprehensive Metabolic Screening for Newborn Health
The Newborn Screening Panel NBS Quad Test represents a cornerstone of preventive pediatric healthcare, designed to identify four critical inherited metabolic disorders within the first days of an infant’s life. This essential screening program has been implemented nationwide to detect conditions that, if left untreated, could lead to severe developmental delays, intellectual disabilities, or life-threatening complications. The test’s importance lies in its ability to identify these disorders before symptoms manifest, allowing for early intervention that can completely prevent the devastating consequences of these conditions.
What the NBS Quad Test Measures
This comprehensive screening panel utilizes advanced fluoroimmunoassay technology to detect four specific metabolic markers:
- TSH (Thyroid-Stimulating Hormone) – Screens for congenital hypothyroidism, a condition where the thyroid gland doesn’t produce enough hormones essential for brain development and growth
- 17-Hydroxyprogesterone – Detects congenital adrenal hyperplasia, a disorder affecting adrenal gland function and hormone production
- Phenylalanine – Identifies phenylketonuria (PKU), an inherited metabolic disorder that prevents proper breakdown of the amino acid phenylalanine
- Galactosemia markers – Screens for galactosemia, a condition where the body cannot process galactose, a sugar found in milk
Who Should Consider This Test
The Newborn Screening Panel NBS Quad Test is recommended for:
- All newborns within 24-48 hours of birth
- Infants born to parents with family histories of metabolic disorders
- Babies showing early signs of feeding difficulties or lethargy
- Infants with siblings diagnosed with metabolic conditions
- All infants regardless of apparent health status, as these conditions often show no initial symptoms
Critical Benefits of Early Screening
Early detection through the NBS Quad Test provides numerous life-changing benefits:
- Prevents irreversible brain damage through timely intervention
- Avoids developmental delays and intellectual disabilities
- Prevents life-threatening metabolic crises
- Enables normal growth and development with appropriate treatment
- Provides peace of mind for parents and caregivers
- Reduces long-term healthcare costs through early intervention
- Supports optimal neurological development during critical early months
Understanding Your Test Results
Your NBS Quad Test results will fall into one of three categories:
- Normal Results – All four markers fall within expected ranges, indicating no detected metabolic disorders. Regular pediatric follow-up is still recommended.
- Borderline/Repeat Testing Required – Some markers may require additional testing for confirmation. This doesn’t necessarily indicate a problem but ensures accuracy.
- Abnormal Results – Positive findings require immediate consultation with a pediatric genetic specialist for confirmatory testing and treatment planning.
All abnormal results are followed by immediate notification and referral to appropriate specialists for comprehensive evaluation and management.
Test Pricing and Availability
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Newborn Screening Panel NBS Quad Test | $30 USD | $32 USD |
Nationwide Accessibility
We maintain comprehensive testing facilities across the United States, with convenient locations in major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and numerous other cities. Our network ensures that every newborn has access to this life-saving screening regardless of geographic location.
Take Action for Your Newborn’s Health
Don’t leave your infant’s health to chance. The Newborn Screening Panel NBS Quad Test provides essential protection against four serious metabolic disorders that can have lifelong consequences if undetected. With rapid next-day results and affordable pricing at only $30, there’s no reason to delay this critical screening.
Book your newborn’s screening today by calling our dedicated pediatric genetics team at +1(267) 388-9828 or schedule your appointment online. Early detection saves lives and ensures your baby’s healthy development.
