Severe G6PD Deficiency Due to a New Missense Mutation in an Infant of Northern European Descent.
2015
We report a term male infant born to parents of Danish descent, who on the second day of life developed jaundice peaking at 67 hours and decreasing on applied double-sided phototherapy. In the weeks following, the infant showed signs of ongoing hemolysis. Laboratory tests showed very low glucose-6-p
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