Newborn Screening Panel Basic Test
Comprehensive Newborn Health Screening for Early Detection
The Newborn Screening Panel Basic Test represents a cornerstone of pediatric preventive healthcare, designed to identify potentially serious medical conditions in infants before clinical symptoms manifest. This essential screening program utilizes advanced diagnostic technologies to detect metabolic, endocrine, and hematological disorders that, if left untreated, could lead to severe developmental delays, intellectual disabilities, or life-threatening complications.
What Does the Newborn Screening Panel Measure?
Our comprehensive basic screening panel evaluates four critical health markers through sophisticated laboratory analysis:
- TSH (Thyroid-Stimulating Hormone): Screens for congenital hypothyroidism, a condition where the thyroid gland doesn’t produce sufficient hormones, potentially affecting brain development and growth
- 17-Hydroxyprogesterone: Detects congenital adrenal hyperplasia, an inherited disorder affecting adrenal gland function and hormone production
- G6PD (Glucose-6-Phosphate Dehydrogenase): Identifies G6PD deficiency, an enzyme disorder that can cause hemolytic anemia when exposed to certain medications or foods
- Hemoglobinopathy: Screens for inherited blood disorders including sickle cell disease and thalassemia, which affect hemoglobin structure and function
Who Should Consider This Essential Screening?
The Newborn Screening Panel Basic Test is recommended for:
- All newborns within the first 24-48 hours of life
- Infants born to families with history of metabolic disorders
- Babies showing no apparent symptoms but at risk for inherited conditions
- Newborns requiring comprehensive baseline health assessment
- Infants born prematurely or with low birth weight
Critical Benefits of Early Newborn Screening
Early detection through newborn screening provides numerous advantages:
- Prevention of Developmental Delays: Early intervention can prevent intellectual disability and growth problems
- Life-Saving Treatment: Timely diagnosis allows for immediate medical management of serious conditions
- Reduced Healthcare Costs: Early treatment is significantly more cost-effective than managing advanced disease complications
- Family Planning Guidance: Identifies inherited conditions that may affect future pregnancies
- Peace of Mind: Provides reassurance about your baby’s health status
Understanding Your Test Results
Your newborn screening results will be carefully interpreted by our genetic specialists:
- Normal Results: Indicate no detected abnormalities in the screened conditions
- Borderline Results: May require repeat testing or additional evaluation
- Abnormal Results: Prompt immediate referral to pediatric specialists for confirmatory testing and treatment initiation
- Follow-up Protocol: All abnormal results trigger immediate notification and coordination with your pediatrician
Test Pricing and Availability
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Newborn Screening Panel Basic Test | $40 USD | $46 USD |
Nationwide Accessibility
We proudly serve families across the United States with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many more cities. Our network of certified collection centers ensures accessible newborn screening services nationwide.
Schedule Your Newborn Screening Today
Don’t leave your baby’s health to chance. Early detection through comprehensive newborn screening can make a lifetime of difference. Our experienced pediatric genetic specialists are ready to provide the highest quality care for your newborn.
Call or WhatsApp us today at +1(267) 388-9828 to schedule your newborn screening appointment or to speak with our genetic counseling team about this essential health screening.
Sample Requirements: 1 drop of heel prick blood each on 3 spots of filter paper. Samples accepted Monday, Wednesday, Friday by 9 AM with next-day results available. Clinical details and medication history must accompany all samples.
