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A newborn genetic screening is a test that is done on every newborn to check for certain genetic disorders. The newborn screening test is conducted for every baby within 24-48 hours of the birth. The test involves taking a sample of blood from the baby’s heel and then sending it off to a lab for analysis. The test helps both the parents and doctors to diagnose the condition and take timely measurements to manage, intervene or treat the disease. This will help the baby lead a healthy and happy life. Trivitron health care manufacture and supplies newborn screening kits for universal newborn screening. Visit us: Ph: +91 - 44 - 2498 5050, 4347 7800 Email: [email protected] Web : https://www.trivitron.com/products/newborn-screening

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