Fetal cfDNA testing can reduce unnecessary care during pregnancy
Fetal cfDNA testing can determine if a fetus lacks an antigen that could cause HDFN, avoiding further unnecessary tests and anxiety.
Fetal cfDNA testing can determine if a fetus lacks an antigen that could cause HDFN, avoiding further unnecessary tests and anxiety.
Comprehensive Rh blood typing and genetic analysis can help prevent HDFN and reduce transfusion-related complications.
Better transfusion record sharing through the Alloantibody Exchange can prevent dangerous delays in identifying antibodies that cause HDFN.
Most infants in the study with Rh-linked hemolytic disease were born with high iron levels that can persist for up to a year.
A review of 238 studies on HDFN showed 104 different outcomes reported with major differences in how they were defined and measured.
Infants with severe neonatal jaundice, a symptom of HDFN, showed higher blood levels of a heart injury marker in a recent study.
A Nigerian study found that nearly 5% of pregnant women carried antibodies that could cause hemolytic disease of the fetus and newborn.
A recent study found no cases of HDFN or autoimmune hemolytic anemia in women or their children despite the presence of these antibodies.
Newborns with HDFN face a greater risk of necrotizing enterocolitis, a dangerous intestinal condition, especially after certain treatments.
Genetic blood testing can spot rare blood type differences that standard tests may miss, which could help prevent HDFN.