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Newborn Screening: Uncovering Rare Diseases and Providing Hope

03 - July - 2023

Newborn screening is a very important step after the baby is born. Read this article to understand its role and relevance with baby’s health.

Newborn screening is a vital process that helps identify rare but serious medical conditions in infants shortly after birth. The sample collection procedure is non-invasive and involves a few drops of blood from newborns between 48-72 hours of birth. Blood testing can provide early detection and intervention for potential defects and disabilities (both mental and physical) and sometimes life-threatening conditions. By detecting these diseases early, healthcare professionals can initiate timely & immediate treatments, improving outcomes, offering healthy life to babies, and bringing down anxiety in affected families. In this article, two experts share their insights about the topic and importance of newborn screening.

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