Hemoglobinuria associated with hemolytic disease of the newborn infant

Joseph J. Angella; Ernesto N. Prieto; Bernard J. Fogel

doi:10.1016/S0022-3476(67)80103-3

Hemoglobinuria associated with hemolytic disease of the newborn infant

Joseph J. Angella, Ernesto N. Prieto, Bernard J. Fogel

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Abstract

An infant with ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency developed severe intravascular hemolysis leading to hemoglobinuria in the immediate neonatal period. Severe intravascular hemolysis with resultant hemoglobinuria is rare in ABO hemolytic disease of the newborn. In vitro studies of the maternal serum demonstrated a complement dependent antibody which was capable of lysing normal B-positive erythrocytes.

Original language	English (US)
Pages (from-to)	530-533
Number of pages	4
Journal	The Journal of Pediatrics
Volume	71
Issue number	4
DOIs	https://doi.org/10.1016/S0022-3476(67)80103-3
State	Published - Oct 1967

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

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10.1016/S0022-3476(67)80103-3

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title = "Hemoglobinuria associated with hemolytic disease of the newborn infant",

abstract = "An infant with ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency developed severe intravascular hemolysis leading to hemoglobinuria in the immediate neonatal period. Severe intravascular hemolysis with resultant hemoglobinuria is rare in ABO hemolytic disease of the newborn. In vitro studies of the maternal serum demonstrated a complement dependent antibody which was capable of lysing normal B-positive erythrocytes.",

author = "Angella, {Joseph J.} and Prieto, {Ernesto N.} and Fogel, {Bernard J.}",

year = "1967",

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language = "English (US)",

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T1 - Hemoglobinuria associated with hemolytic disease of the newborn infant

AU - Angella, Joseph J.

AU - Prieto, Ernesto N.

AU - Fogel, Bernard J.

PY - 1967/10

Y1 - 1967/10

N2 - An infant with ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency developed severe intravascular hemolysis leading to hemoglobinuria in the immediate neonatal period. Severe intravascular hemolysis with resultant hemoglobinuria is rare in ABO hemolytic disease of the newborn. In vitro studies of the maternal serum demonstrated a complement dependent antibody which was capable of lysing normal B-positive erythrocytes.

AB - An infant with ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency developed severe intravascular hemolysis leading to hemoglobinuria in the immediate neonatal period. Severe intravascular hemolysis with resultant hemoglobinuria is rare in ABO hemolytic disease of the newborn. In vitro studies of the maternal serum demonstrated a complement dependent antibody which was capable of lysing normal B-positive erythrocytes.

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DO - 10.1016/S0022-3476(67)80103-3

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JO - Journal of Pediatrics

JF - Journal of Pediatrics

SN - 0022-3476

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ER -

Hemoglobinuria associated with hemolytic disease of the newborn infant

Abstract

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