Dataset of Six Congenital Disorders Detected Through Newborn Screening in Northwest Mexico (2012–2023)

This dataset contains information on 3,458 newborns identified as suspected cases through the neonatal screening program at <i>Hospital de la Mujer</i> in Culiacán, Sinaloa, Mexico, between January 1, 2012, and December 31, 2023. It includes both demographic and clinical data related to mothers and newborns.<b>Maternal information</b> comprises age, number of births, geographic location, and gestational age.<br><b>Newborn data</b> includes date of birth, sex, birth weight, and birth length.<br><b>Newborn screening information</b> covers the date of blood sample collection, suspected congenital disorders, and confirmatory test results for the six conditions screened.<br><b>Congenital Disorders: </b>congenital hypothyroidism (CH), congenital adrenal hyperplasia (CAH), galactosemia (GALA), phenylketonuria (PKU), cystic fibrosis (CF), and glucose-6-phosphate dehydrogenase deficiency (G6PDd).<br>The authors kindly ask that proper credit be given in future uses or publications that utilize this dataset.