info@vjscans.in
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Our Newborn Screening division is dedicated to the early detection of congenital disorders that can affect a childs long-term health. We utilize advanced screening technologies to identify metabolic, genetic, and hormonal conditions within days of birth, empowering parents and clinicians with the vital information needed for timely intervention and optimal development.
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Why Newborn Screening:
A Vital Step for Your Baby
Newborn screening identifies conditions that can affect a childs long-term health or survival. Early detection, diagnosis, and intervention can prevent death or disability and enable children to reach their full potential.
- Identifies metabolic, hormonal, and genetic disorders early upon birth
- Prevents severe developmental delays and health complications
- Early treatment ensures a healthier, normal life
- Simple, safe, and quick heel-prick test
- Recommended for every newborn baby
- Peace of mind for parents regarding hidden conditions
Conditions We Screen For
Metabolic Disorders
- Phenylketonuria (PKU)
- Galactosemia
- Fatty Acid Oxidation Disorders
- Organic Acidemias
Hormonal Disorders
- Congenital Hypothyroidism
- Congenital Adrenal Hyperplasia
- Thyroid Function Issues
- Growth Hormone Deficiency
Hemoglobinopathies
- Sickle Cell Disease
- Thalassemia
- Hemoglobin Variants
- Other Blood Disorders
Expert Detection Methodologies
Tandem Mass Spectrometry (MS/MS) for metabolic profile
Enzyme-linked Immunosorbent Assay (ELISA)
High-Performance Liquid Chromatography (HPLC)
Molecular Genetic Testing (DNA Analysis)
Automated Fluorometric Assays
Rapid turnaround time for critical conditions
High sensitivity and specificity
Comprehensive panel covering 50+ disorders
Expert interpretation by biochemical geneticists
confirmatory testing for positive screens
Why Early Screening Matters
We provide a complete range of diagnostic ultrasound scans using advanced 2D, 3D, and Doppler technology for accurate and safe results.
Ensures your baby gets a healthy start to life.
Detects hidden conditions before symptoms appear.
Allows for immediate treatment to prevent damage.
Simple, safe, and non-invasive procedure.
Prevents long-term physical and mental disability.
Peace of mind for new parents.
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Frequently Asked Questions
Common questions about our services and procedures.
It identifies potential health issues early, allowing for immediate treatment that can prevent severe health problems or developmental delays.
The ideal time for newborn screening is between 24 and 48 hours after birth for the most accurate results.
The test involves a quick heel prick which may cause momentary discomfort, but it is safe and crucial for your baby's health.
Results are typically available within 3-5 days. Your doctor will contact you immediately if any abnormalities are found.
A positive result means further testing is needed to confirm a diagnosis. It does not always mean your baby has the condition.
