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The page below is a sample from the LabCE course Hemolytic Disease of the Fetus and Newborn. Access the complete course and earn ASCLS P.A.C.E.-approved continuing education credits by subscribing online.

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RhIg and Rh Complexity

Policies for administering RhIg when the mother's Rh type is weak D vary among countries and within some countries.

To understand the issues involved, we need to review the genetics of the Rh D antigen and the types of weak D (formerly Du). The Rh system is complex and only a basic overview will be given.

In brief, Rh system inheritance is determined by two sets of genes:

  • RHD codes for the proteins carrying D expression. In most people, the presence or absence of the RHD gene results in being Rh positive or Rh negative, respectively.
  • RHCE codes for different combinations of the proteins carrying CcEe expression and Rh-associated glycoprotein (RhAG). RhAG is needed for the expression of Rh antigens. The RHCE locus is adjacent to RHD on chromosome #1.
  • See a model for the Rh locus (NCBI)

D variants

For a small percentage of people, the inheritance of the RHD gene and the expression of the D antigen may be altered leading to several variants of D encoded by more than 100 RHD alleles