neonatal period is the period up until
4 weeks
neonatal jaundice can be
physiological or pathological
physiological jaunidce
nearly all babies are born with some physiological jaundice the baby transitions from relying on the placenta to clear bilirubin to using its own hepatic system
physiological jaundice is never visible
in the first day of life and if a neonate has jaundice within the first 24 hours f life there is always a pathological cause
in physiological jaundice
levels of conjugated bilirubin never suprasses
physiological jaundice normally resolved within
- 2 weeks in a premature infant
premature infant
gestation less than 37 weeks
prolonged jaundice
- 21 days or more in pre-term infant
pathological jaundice definition
any jaundice that does not satisfy the criteria of being physiological jaundice
causes of pathological jaundice
Rh incompatibility
when a Rh negative mother has a resus positive child she produced Rh autoantibodies so if she has another pregnancy with a Rh positive baby the antibodies attack the foetus
ABO incompatibility
attack on red blood cells by maternal anti-ABO antibodies
Crigler Najjar syndrome
absence of the enzyme UGT1A1 resulting in the inability to conjugate bilirubin causing an indirect hyperbilirunaemia
biliary atresia
only prevents in neonates, defect in biliary tract which causes cholestasis, conjugated bilirubin is absorbed into the bloodstream as it cannot be transported into the duodenum therefore= direct hyperbilirunaemia
UTIS in neonates
UTI in neonates is associated with bacteramiea and congenital anomalies in the kidney and urinary tract
congenital hypothyroidism
INADEQUATE THYROID HORMONE PRODUCTION IN NEWBORN INFANT
Cause of congenital hypothyroidism
congenital hypothyroidism is the
most common neonatal endocrine disorder
symptoms of neonatal hypothyroidism
decreased activity, large anterior fontanelle, constipation, weight gain, jaundice, hypotonia, poor feeding
if congenital hypothyroidism goes untreated it causes
CRETINISM: severely stunted physical and mental development
if hypothyroidism remains untreated in a mother during pregnancy causes
gallactosemia
mutations in GALT, GALK1 AND GALE GENES, result in inability to process galactose, as these genes code for the enzymes that break down galactose
classic galactossemia is
type 1 which is the most common and most severe type if they are not treated with a galactose free diet it can be life-threatening causing failure to gaibn weight and growth, jaundice, liver damage and abnormal bleeding
breast milk intolerance
neonatal jaundice associated with breast feeding characterised by indirect hyperbilurinaemia in an otherwise healthy breastfed newborn where there is no other identifiable cause