A rare genetic deletion in a blood group gene caused hemolytic disease of the fetus and newborn (HDFN) in twin infants.
In a recent study, parents of infants with HDFN reported feelings of uncertainty and distress regarding post-discharge care.
About one in three babies in Africa are born with anemia, a condition in which a baby’s blood doesn’t have enough healthy red ...
Fetal cfDNA testing can determine if a fetus lacks an antigen that could cause HDFN, avoiding further unnecessary tests and ...
Despite advances in screening and treatment, HDFN remains a significant cause of perinatal morbidity and mortality worldwide.
A study showed babies who have ABO-mediated HDFN should be checked for signs of jaundice two to three times during the first ...
A pregnancy affected by HDFN due to rare antibodies was successfully managed, and the affected infant was born without serious complications.
A recent study found that phototherapy induces chemical changes to bilirubin that may lead to inaccurate and nonsensical measurements.
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