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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 ...
Cell-free DNA can be used the determine the Rh antigen of the fetus when the mother is Rh negative. Blood is taken from the mother during the pregnancy, and using PCR, can detect the K, C, c, D, and E alleles of fetal DNA. This blood test is non-invasive to the fetus and is an easy way of checking antigen status and risk of HDN.
Hemolytic disease of the newborn, also known as hemolytic disease of the fetus and newborn, HDN, HDFN, or erythroblastosis fetalis, [1] [2] is an alloimmune condition that develops in a fetus at or around birth, when the IgG molecules (one of the five main types of antibodies) produced by the mother pass through the placenta.
Once a woman has antibodies, she is at high risk for a transfusion reaction. [10] For this reason, she must carry a medical alert card at all times and inform all doctors of her antibody status. [citation needed] "Acute hemolytic transfusion reactions may be either immune-mediated or nonimmune-mediated.
The anti-RhE antibody is quite common especially in the Rh genotype CDe/CDe; it usually only causes a mild hemolytic disease, but can cause a severe condition in the newborn. It can occur with other antibodies, usually the anti-Rhc antibody, which can also cause a severe hemolytic disease. [1]
In about a third of all ABO incompatible pregnancies maternal IgG anti-A or IgG anti-B antibodies pass through the placenta to the fetal circulation leading to a weakly positive direct Coombs test for the neonate's blood. [citation needed] However, ABO HDN is generally mild and short-lived and only occasionally severe because:
Rh disease (Rh D) [1] ABO hemolytic disease of the newborn [1] Anti-Kell hemolytic disease of the newborn [1] Rhesus c hemolytic disease of the newborn [1] Rhesus E hemolytic disease of the newborn [1] Other blood group incompatibility (RhC, Rhe, Kidd, Duffy, MN, P and others) [1]
Rh incompatibility; Sacrococcygeal teratoma; Spina bifida; Spinal dysraphism; Syndactyly; Tetralogy of Fallot; Thanatophoric dwarfism; Transposition of the great vessels; Triploidy; Trisomy 13; Trisomy 18; Trisomy 21 (Down Syndrome) Turner syndrome (Monosomy X) Twin-to-twin transfusion syndrome; Ureterocele; VACTERL association; Vein of Galen ...