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Newborn Screening Panel 2 Test

Original price was: $16.Current price is: $14.

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The Newborn Screening Panel 2 Test is a comprehensive genetic screening designed to detect critical metabolic and genetic disorders in newborns. This advanced panel specifically measures TSH levels for thyroid function assessment and G-6PD enzyme activity for glucose-6-phosphate dehydrogenase deficiency detection. Early identification of these conditions allows for timely intervention and treatment, preventing serious developmental complications. The test requires only a small heel prick blood sample collected on specialized filter paper. Results are typically available the next day when samples are submitted Monday through Friday by 9 AM. This affordable screening costs only $14 USD and provides invaluable peace of mind for parents concerned about their newborn’s genetic health. Our nationwide network of testing facilities ensures convenient access across all major US cities.

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Newborn Screening Panel 2 Test: Comprehensive Genetic Screening for Your Newborn

Introduction to Newborn Screening Panel 2

The Newborn Screening Panel 2 represents a crucial advancement in pediatric healthcare, offering comprehensive genetic screening designed to detect potentially life-threatening metabolic and genetic disorders during the earliest stages of life. This specialized panel utilizes cutting-edge fluoroimmunoassay technology to provide accurate, reliable results that can significantly impact your newborn’s long-term health outcomes. Early detection through this screening allows healthcare providers to implement timely interventions that can prevent serious developmental delays, intellectual disabilities, and other complications associated with undiagnosed genetic conditions.

What Does the Newborn Screening Panel 2 Measure?

This comprehensive screening panel specifically targets two critical components that are essential for your newborn’s healthy development:

Thyroid-Stimulating Hormone (TSH) Assessment

  • Measures thyroid function and detects congenital hypothyroidism
  • Identifies potential thyroid hormone deficiencies that could affect growth and brain development
  • Provides early warning for conditions that might impact metabolic rate and overall development

Glucose-6-Phosphate Dehydrogenase (G-6PD) Enzyme Analysis

  • Detects G-6PD deficiency, a common enzyme disorder affecting red blood cells
  • Identifies susceptibility to hemolytic anemia triggered by certain foods, medications, or infections
  • Provides crucial information for medication safety and dietary considerations

Who Should Consider This Screening?

The Newborn Screening Panel 2 is recommended for all newborns as part of comprehensive pediatric care. Specific indications include:

  • All newborns within the first few days of life
  • Infants with family history of metabolic disorders
  • Babies showing early signs of feeding difficulties or lethargy
  • Newborns from populations with higher prevalence of G-6PD deficiency
  • Infants requiring baseline genetic health assessment

Benefits of Newborn Screening Panel 2

Early detection through this comprehensive screening offers numerous advantages:

  • Prevention of Developmental Delays: Early intervention can prevent intellectual disabilities and growth problems
  • Timely Treatment Initiation: Allows for immediate medical management when conditions are detected
  • Family Planning Guidance: Provides valuable genetic information for future family planning
  • Peace of Mind: Offers reassurance to parents about their newborn’s genetic health status
  • Cost-Effective Healthcare: Prevents expensive long-term treatments through early detection

Understanding Your Test Results

Your Newborn Screening Panel 2 results will be carefully interpreted by our genetic specialists:

Normal Results

Normal TSH and G-6PD levels indicate that your newborn shows no evidence of the screened conditions at the time of testing. Regular pediatric follow-up is still recommended.

Abnormal Results

Abnormal findings will trigger immediate notification and referral to appropriate specialists for confirmatory testing and treatment planning. Our genetic counselors are available to help you understand the implications and next steps.

Borderline Results

Some results may fall in borderline ranges, requiring repeat testing or additional monitoring. Our team will provide clear guidance on appropriate follow-up procedures.

Test Information and Pricing

Test Component Details
Test Name Newborn Screening Panel 2
Regular Price $16 USD
Discount Price $14 USD
Turnaround Time Sample Monday through Friday by 9 AM; Report Next Day
Sample Type 1 drop of heel prick blood each on 3 spots of filter paper
Specialty Pediatric Genetics
Method Fluoroimmunoassay

Nationwide Testing Availability

We have branches across the United States, ensuring convenient access to the Newborn Screening Panel 2 in all major cities including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more. Our network of certified collection facilities provides consistent, high-quality service nationwide.

Book Your Newborn Screening Today

Don’t leave your newborn’s genetic health to chance. The Newborn Screening Panel 2 offers affordable, comprehensive screening that can make a lifetime of difference. Our experienced genetic specialists and pediatric consultants are ready to assist you with scheduling and answer any questions you may have about the testing process.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your newborn’s screening appointment. Take the first step toward ensuring your baby’s healthy future with this essential genetic assessment.