Prematurity (the risk increases with each additional week below 40 weeks) |
Hemolytic disorders (eg, alloimmune HDN, G6PD deficiency, other inherited hemolytic conditions) |
Early-onset of jaundice (within first 24 hours after birth) |
Parent or sibling who required treatment for neonatal jaundice |
Family history or ancestry suggestive of an inherited hemolytic disorder (ie, G6PD deficiency, hereditary spherocytosis) |
Bruising, cephalohematoma, or internal bleeding |
Macrosomia in a newborn of a diabetic mother |
Down syndrome |
Exclusive breastfeeding (with suboptimal intake) |
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