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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Erythroblastosis, Fetal
Immune System Diseases > Erythroblastosis, Fetal
Hemic and Lymphatic Diseases > Hematologic Diseases > Erythroblastosis, Fetal
Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Pregnancy Complications > Fetal Diseases > Erythroblastosis, Fetal
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Fetal Diseases > Erythroblastosis, Fetal

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Erythroblastosis, Fetal  

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Tipo

  • mesh:Descriptor

Definición

  • A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP INCOMPATIBILITY, such as the maternal alloimmunization by fetal antigen RH FACTORS leading to HEMOLYSIS of ERYTHROCYTES, hemolytic anemia (ANEMIA, HEMOLYTIC), general edema (HYDROPS FETALIS), and SEVERE JAUNDICE IN NEWBORN.

Concepto genérico

Conceptos específicos

Conceptos relacionados

Etiquetas alternativas

  • Erythroblastosis Fetalis
  • Hemolytic Disease of Newborn

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-F5QMLCFQ-L

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