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Clin Ter ; 165(3): 151-4, 2014.
Article in English | MEDLINE | ID: mdl-24999569

ABSTRACT

ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency G6PD are common haematological problems affecting the newborn. The resulting haemolytic disease of foetus and newborn (HDFN) caused by either of these pathologies generally follows a benign course. It is typically characterized by mild jaundice without significant anaemia. ABO incompatibility alone as a cause of foetal hydrops is extremely rare. We report a case of a newborn baby girl with an anti-B isoimmunisation and G6PD deficiency manifesting with hydrops foetalis, anaemia and hyperbilirubinaemia, born to a mother with blood group O.


Subject(s)
Blood Group Incompatibility , Glucosephosphate Dehydrogenase Deficiency/etiology , Hydrops Fetalis/etiology , Anemia/etiology , Female , Humans , Hydrops Fetalis/diagnostic imaging , Hyperbilirubinemia/etiology , Infant, Newborn , Pregnancy , Ultrasonography
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