Search results
Results From The WOW.Com Content Network
Rh disease (also known as rhesus isoimmunization, Rh (D) disease, or rhesus incompatibility, and blue baby disease) is a type of hemolytic disease of the fetus and newborn (HDFN). HDFN due to anti-D antibodies is the proper and currently used name for this disease as the Rh blood group system actually has more than 50 antigens and not only the ...
Splenomegaly, cardiomegaly and hepatomegaly may occur in the baby. [5] Excessive tissue fluid may accumulate in the stomach, lungs or scalp. These are typically signs of hydrops fetalis. [5] After birth, the symptoms of the child are similar to that of incompatible blood transfusion in adults. The baby may have pale skin due to anaemia.
Hemolytic disease of the newborn (anti-Rhc) can range from a mild to a severe disease. It is the third most common cause of severe HDN. Rh disease is the most common and hemolytic disease of the newborn (anti-Kell) is the second most common cause of severe HDN. It occurs more commonly in women who are Rh D negative. [citation needed]
Hemolytic disease of the fetus and newborn (HDN) is a condition where the passage of maternal antibodies results in the hemolysis of fetal/neonatal red cells. The antibodies can be naturally occurring such as anti-A, and anti-B, or immune antibodies developed following a sensitizing event. [ 12 ]
If you don’t have the “Rh factor” in your blood, you risk having a baby with rhesus disease (Rh disease). Here’s what you need to know about being Rh-negative in pregnancy.
Hemolytic disease of the newborn (anti-Kell 1) is caused by a mismatch between the Kell antigens of the mother and fetus. About 91% of the population are Kell 1 negative and about 9% are Kell 1 positive. A fraction of a percentage are homozygous for Kell 1. Therefore, about 4.5% of babies born to a Kell 1 negative mother are Kell 1 positive ...
Babies and other young children, as well as the elderly and people with chronic kidney and heart problems, need to visit the doctor sooner rather than later to make sure they are keeping hydrated.
Vos originally described Rh-deficiency syndrome in 1961, when a sample of blood failed to respond with several Rh antisera. However, R. Ceppellini used the term "Rhnull" for the first time. So far, at least 43 people from 14 families have been reported in the literature as having the Rhnull phenotype.