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Objective: The basic screening of newborn babies for detecting pathologies like G6PD deficiency leading to hyperbilirubinemia, congenital adrenal hyperplasia and congenital hypothyroidism. Method: A Screening Program was conducted at a tertiary care hospital for 2 months i.e. April 2014 to May 2014. All the neonates born in this hospital were screened on third to fifth day oftheir birth for levels of Glucose-6-Phosphate Dehydrogenase (G6PD), 17Hydroxyprogesterone (17-OHP) and Thyroid Stimulating Hormone (TSH). Results: Out of a total of 57 neonates screened in 2 months, 2 cases (4.26%, 1 male and 1 female) were observed as G6PD deficient and no cases were observed for increased level 17-OHP and increased level of TSH. Conclusion:   Neonatal screening is very important in reducing neonatal mortality and morbidity. Screening programs help us to identify those cases that cannot be identified by routine observation and physical examination. A cost effective nation wide screening program is highly recommended for detection of cases as early as possible.

Neonatal Screening for G6PD, 17-OHP and TSH Levels