erythroblastosis fetalis

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Related to hemolytic disease of newborn: erythroblastosis fetalis

erythroblastosis fe·ta·lis

 (fē-tā′lĭs)
n.
A severe hemolytic disease of a fetus or newborn infant caused by the production of maternal antibodies against the fetal red blood cells, usually involving Rh incompatibility between the mother and fetus. Also called RH disease.

[New Latin erythroblastōsis fētālis : erythroblastōsis, erythroblastosis + fētālis, fetal.]
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.erythroblastosis fetalis - severe anemia in newborn babies; the result of Rh incompatibility between maternal and fetal blood; typically occurs when the child of an Rh-negative mother inherits Rh-positive blood from the father; can be diagnosed before birth by amniocentesis
anemia, anaemia - a deficiency of red blood cells
References in periodicals archive ?
Endovenous immunoglobulin in Rh hemolytic disease of newborn.
Subjects and Methods: A structured questionnaire was used to assess the knowledge regarding Rh disease and hemolytic disease of newborn, after taking informed written consent.
6 per 1000 live births for ABO Hemolytic disease of newborn in two hospital based studies from Bombay (8).

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