enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Rh disease - Wikipedia

    en.wikipedia.org/wiki/Rh_disease

    The fetal Rh can be screened using non-invasive prenatal testing (NIPT). This test can screen for the fetus's Rh antigen (positive or negative) at the 10th week of gestation using a blood sample drawn from the mother. The Unity test uses NGS technology to look for Rh alleles (genes) in the cell free fetal DNA in the maternal bloodstream. In ...

  3. Hemolytic disease of the newborn (anti-Kell) - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_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.

  4. Hemolytic disease of the newborn (anti-Rhc) - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_the...

    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.

  5. Rho (D) immune globulin - Wikipedia

    en.wikipedia.org/wiki/Rho(D)_immune_globulin

    The RhD status of the fetus is determined by genetic inheritance. In a pregnancy where the mother is RhD negative and the father is RhD positive, the probability of the fetus having RhD positive blood is dependent on whether the father is homozygous for RhD (i.e., both RhD alleles are present) or heterozygous (i.e., only one RhD allele is ...

  6. Rh deficiency syndrome - Wikipedia

    en.wikipedia.org/wiki/Rh_deficiency_syndrome

    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. [4]

  7. Hemolytic disease of the newborn - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_the...

    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.

  8. Kell antigen system - Wikipedia

    en.wikipedia.org/wiki/Kell_antigen_system

    Anti-K is the next most common immune red cell antibody after those in the ABO and Rh system. Anti-K typically presents as IgG class alloantibody. Individuals lacking a specific Kell antigen may develop antibodies against Kell antigens when transfused with blood containing that antigen. This is particularly true for the "K" antigen which shows ...

  9. Hemolytic disease of the newborn (anti-RhE) - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_the...

    In some cases, the direct Coombs will be negative but severe, even fatal HDN can occur. [29] An indirect Coombs needs to be run in cases of anti-C, [30] anti-c, [30] and anti-M. Anti-M also recommends antigen testing to rule out the presence of HDN. [22] Hgb – the infant's hemoglobin should be tested from cord blood. [3]