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Rh Factor Inheritance: Why Two O-Negative Parents Can Only Have O-Negative Children
The Rh blood group system is determined by the RHD gene on chromosome 1. The D antigen (Rh factor) is either present (Rh-positive) or absent (Rh-negative).
Genetics
- Rh-Positive: At least one functional RHD allele (DD or Dd).
- Rh-Negative: Two deleted/nonfunctional RHD alleles (dd).
O-Negative Parents (Genotype: OO dd)
- ABO: Both ii → only i allele to transmit.
- Rh: Both dd → only d allele to transmit.
Offspring Genotype
ABO: i × i → ii (Type O) — 100% Rh: d × d → dd (Rh-negative) — 100%
Result: All children will be Type O, Rh-negative (O negative).
Exceptions (Vanishingly Rare)
- RHD Gene Rearrangement: Partial D, weak D, Del — serologically Rh-negative but genetically variant.
- Chimerism: Two zygotes fuse → two cell lines.
- Somatic Mutation / Gene Conversion: Theoretical.
- Lab Error / Non-Paternity: Most common "explanation."
Clinical Note
Rh-negative mothers carrying Rh-positive fetuses (from Rh-positive father) risk alloimmunization → HDFN. Rho(D) immune globulin (RhoGAM) at 28 weeks and postpartum prevents this. Two Rh-negative parents eliminate this risk entirely.
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