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Hemolytic disease of the newborn is also known as erythroblastosis fetalis. It is a condition that develops in a fetus when the mother and fetus have incompatible blood types.
Hemolytic disease of the newborn is known as erythroblastosis fetalis
An aetiopathogenesis is the cause or subsequent development of a abnormal condition or disease.
Approximately 40% of the patients have a history of inflammation of a vein (phlebitis), which may play a role in the development of Buerger's disease.
Umm, no. You're either born with or without Down syndrome. It's not a disease, it's a genetic condition.
A hemolytic disease of the newborn that is characterized by an increase in circulating red blood cells and by jaundice and that occurs when the system of an Rh-negative mother produces antibodies to an antigen in the blood of an Rh-positive fetus which cross the placenta and destroy fetal red blood cells, called also hemolytic disease of the newborn.
hemolytic anemia
This is a condition in which there is abnormal destruction of the red blood cells of the baby. It can be due to blood group incompatibility between mother and baby or due to diseases of red blood cells in the baby.
Hirschsprung's disease is a congenital abnormality that has no known means of prevention. It is important to diagnose the condition early in order to prevent the development of enterocolitis.
hemolytic anemia and bone marrow
Erythroblastosis fetalis (hemolytic disease of the newborn). A first-born child will not usually suffer harmful effects, however subsequent babies will be affected.
Invasive group B streptococcal (GBS) disease is the most common cause of life-threatening infection in newborns.