The Neonatal Screen Test is designed to identify genetic and metabolic disorders in newborns. Early detection ensures timely intervention, reducing the risk of severe health complications. 

The Neonatal Screen Test is designed to identify genetic and metabolic disorders in newborns. Early detection ensures timely intervention, reducing the risk of severe health complications. 

Why Take the Test? 

This test helps: 

• Detect congenital disorders like hypothyroidism and G6PD deficiency. 
• Identify rare metabolic conditions early. 
• Ensure a healthy start for your baby. 

Key Benefits 

• Promotes early diagnosis and treatment. 
• Prevents developmental delays or irreversible damage. 
• Offers a comprehensive health assessment for newborns. 

Prerequisites 

• Ideally conducted within the first few days of birth. 
• Ensure the baby is well-fed and hydrated before sample collection. 

Who Can Avail This Test? 

All newborns should undergo the neonatal screen test as part of standard postnatal care. 

Report Download 

Your baby's test results can be accessed via the Pathkind Labs portal. Simply log in, go to the test history, and download the report.