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J Perinatol ; 33(6): 490-1, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23719252

ABSTRACT

We present a case of a female neonate who had a nonimmune hydrops fetalis and severe hemolytic anemia due to a rare combination of glucose-6-phosphate dehydrogenase (G6PD) deficiency and congenital dyserythropoietic anemia. We conclude that in severe cases with persistent anemia one should search after delivery for a second reason other than G6PD deficiency alone.


Subject(s)
Anemia, Dyserythropoietic, Congenital/diagnosis , Glucosephosphate Dehydrogenase Deficiency/diagnosis , Hydrops Fetalis/diagnosis , Hydrops Fetalis/etiology , Anemia, Dyserythropoietic, Congenital/therapy , Biopsy, Needle , Bone Marrow/pathology , Cesarean Section , Diagnosis, Differential , Erythroid Precursor Cells/pathology , Exchange Transfusion, Whole Blood , Female , Glucosephosphate Dehydrogenase Deficiency/therapy , Hematocrit , Humans , Hydrops Fetalis/therapy , Infant , Infant, Newborn , Jaundice, Neonatal/diagnosis , Jaundice, Neonatal/etiology , Jaundice, Neonatal/therapy , Microscopy, Electron , Phototherapy , Pregnancy
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