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- W125593926 abstract "A newborn boy born at 37 weeks’ gestation was referred to the paediatric cardiology service while in the neonatal intensive care unit because of bradycardia. Maternal history was significant for hypothyroidism treated with levothyroxine, chronic idiopathic thrombocytopenic purpura identified during pregnancy and treated with prednisone, and cholestasis during pregnancy. Bradycardia was initially detected prenatally; however, regular ultrasounds, fetal echocardiogram and biophysical profiles were normal. Maternal testing was negative for antinuclear antibody, anti-Rho and anti-La antibodies. On delivery, the infant’s heart rate was 100 beats/min and he was transferred to a level 2 nursery.On further history, it was noted that the parents were consanguineous (the parents were first cousins, and the maternal grandmother was the sister of the paternal grandfather), and there was a family history of thrombocytopenia in the father, paternal uncle and paternal grandfather. There was no reported history of arrhythmias, sudden death, unexplained car accidents or drownings in the family. The patient’s four-year-old sister was healthy. On examination, the infant did not exhibit any dysmorphic features. Cardiovascular examination was normal, and there were no signs of heart failure. Further investigations established the diagnosis." @default.
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- W125593926 date "2014-03-01" @default.
- W125593926 modified "2023-09-27" @default.
- W125593926 title "Case 1: An infant with a low heart rate" @default.
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- W125593926 doi "https://doi.org/10.1093/pch/19.3.123a" @default.
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