Introduction
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Rh blood group system is the second most important blood group system after ABO.
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It is highly polymorphic, with more than 50 antigens identified.
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Clinically most significant antigen: D antigen
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Major importance in:
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Blood transfusion reactions
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Hemolytic disease of fetus and newborn (HDFN)
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Rh antigens are protein antigens, unlike carbohydrate ABO antigens.
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Present only on red blood cells, not in body secretions.

History
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Discovered in 1940 by Karl Landsteiner and Alexander Wiener
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Rabbits were immunized with Rhesus monkey red cells
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Resulting antibodies agglutinated human red cells
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Initially believed to be same antigen; later clarified as different but related
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Explained:
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Severe transfusion reactions
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Erythroblastosis fetalis
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The term “Rh factor” became widely accepted.
Genetics
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Genes located on chromosome 1 (1p36.11)
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Controlled by two closely linked genes:
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RHD gene → codes for D antigen
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RHCE gene → codes for C/c and E/e antigens
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Genes are inherited as a haplotype
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Rh positivity depends on presence of RHD gene
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Rh negativity usually due to complete deletion of RHD gene
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Unlike ABO:
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No naturally occurring antibodies
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Antibodies develop only after exposure
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Molecular Genetics of Rh System
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RHD and RHCE genes encode transmembrane proteins
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Proteins have:
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10–12 membrane-spanning segments
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Intracellular and extracellular loops
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Small amino acid substitutions cause:
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Weak D
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Partial D
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Other Rh variants
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Rh proteins are closely associated with:
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Rh-associated glycoprotein (RhAG)
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Normal Rh antigen expression requires:
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Functional RHD/RHCE
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Functional RhAG gene
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Nature of Rh Antigens
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Rh antigens are:
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Proteins
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Heat stable
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Enzyme sensitive
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Fully developed at birth
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Not present in saliva or body fluids
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Strongly immunogenic:
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D antigen is one of the most immunogenic antigens known
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Do not activate complement efficiently
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Antibody-coated cells are removed by extravascular hemolysis
D Antigen
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Most important antigen in Rh system
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Present in ~85% of population
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Highly immunogenic:
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1 unit transfusion → ~80% chance of sensitization
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Presence defines Rh positive
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Absence defines Rh negative
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Primary cause of:
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Severe transfusion reactions
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HDFN
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Weak D (Du Antigen)
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Reduced expression of D antigen on RBC surface
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Caused by:
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Amino acid substitutions in transmembrane region
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Not detectable by immediate spin testing
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Detected by:
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Indirect Antiglobulin Test (IAT)
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Characteristics:
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D antigen complete but quantitatively reduced
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Usually do not form anti-D
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Blood bank significance:
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Donors → treated as Rh positive
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Recipients → often treated as Rh negative (policy dependent)
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Partial D Antigen
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D antigen is qualitatively incomplete
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One or more D epitopes are missing
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Caused by:
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Hybrid RHD–RHCE genes
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Individuals may:
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Type as Rh positive
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Still produce anti-D when exposed
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Very important in:
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Pregnancy
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Transfusion medicine
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Treated as Rh negative recipients
Other Variants of Rh System
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Includes:
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Cw, Cx, Ew
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Del phenotype
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Hybrid Rh antigens
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Common in certain ethnic groups
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Often undetected by routine serology
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Require:
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Advanced serological testing
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Molecular genotyping
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Can cause:
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Unexpected alloimmunization
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Delayed hemolytic reactions
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Rh-Null Phenotype
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Complete absence of all Rh antigens
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Extremely rare
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Two types:
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Amorph type – deletion/inactivation of RHD & RHCE
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Regulator type – mutation in RhAG gene
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Clinical features:
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Mild to moderate hemolytic anemia
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Stomatocytosis
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Increased RBC fragility
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Transfusion problems:
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Only Rh-null blood compatible
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Demonstrates structural importance of Rh proteins
Rh Antibodies
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Not naturally occurring
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Formed only after:
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Transfusion
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Pregnancy
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Belong to IgG class
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Cross placenta easily
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Common antibodies:
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Anti-D (most significant)
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Anti-C
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Anti-E
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Anti-c
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Cause:
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Hemolytic transfusion reactions
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HDFN
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Best detected by:
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Indirect Coombs test
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Factors Influencing Rh Immunization
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Volume of antigen exposure
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Immunogenic strength of antigen
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Route of exposure:
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Transfusion > pregnancy
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Genetic makeup of recipient
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ABO incompatibility:
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Reduces Rh immunization
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Frequency of exposure
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Use or absence of anti-D prophylaxis

Functional Role of Rh Antigens
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Not only blood group markers
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Act as:
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Ammonia transport channels
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CO₂ transport facilitators
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Maintain:
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Red cell membrane stability
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Cell shape and deformability
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Loss of Rh proteins leads to:
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Membrane defects
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Reduced RBC survival
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Explains anemia seen in Rh-null individuals
Clinical Significance of Rh System
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Essential in:
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Blood grouping
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Cross-matching
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Antenatal screening
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Anti-D prophylaxis prevents:
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HDFN
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Maternal sensitization
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Molecular Rh typing improves:
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Transfusion safety
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Management of complex cases
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MCQs
1. The Rh blood group system was discovered in:
A. 1935
B. 1937
C. 1940
D. 1945
Answer: C. 1940
2. Discovery of Rh system is credited to:
A. Landsteiner and Levine
B. Wiener and Coombs
C. Landsteiner and Wiener
D. Ehrlich and Pauling
Answer: C. Landsteiner and Wiener
3. Rh blood group system is second in importance after:
A. Kell
B. ABO
C. Lewis
D. Duffy
Answer: B. ABO
4. The most immunogenic antigen of Rh system is:
A. C
B. c
C. E
D. D
Answer: D. D
5. Rh antigens are chemically:
A. Carbohydrates
B. Glycolipids
C. Proteins
D. Lipopolysaccharides
Answer: C. Proteins
6. Rh antigens are located on:
A. Plasma proteins
B. Platelets
C. Red cell membrane
D. Leukocytes
Answer: C. Red cell membrane
7. Genes controlling Rh system are located on chromosome:
A. 6
B. 9
C. 1
D. 19
Answer: C. 1
8. RHD gene encodes which antigen?
A. C
B. E
C. D
D. c
Answer: C. D
9. RHCE gene encodes which antigens?
A. D only
B. C and D
C. C/c and E/e
D. D and E
Answer: C. C/c and E/e
10. Rh-negative phenotype is usually due to:
A. Suppressed gene expression
B. Mutation of RHCE gene
C. Deletion of RHD gene
D. Absence of RhAG protein
Answer: C. Deletion of RHD gene
11. Naturally occurring antibodies are:
A. Present in Rh system
B. Absent in Rh system
C. IgM type
D. Cold reacting
Answer: B. Absent in Rh system
12. Rh antibodies are usually of which class?
A. IgM
B. IgA
C. IgE
D. IgG
Answer: D. IgG
13. Rh antibodies are formed after:
A. Birth
B. Infection
C. Sensitization
D. Vaccination
Answer: C. Sensitization
14. Which Rh antibody most commonly causes HDFN?
A. Anti-E
B. Anti-C
C. Anti-c
D. Anti-D
Answer: D. Anti-D
15. Weak D antigen is best detected by:
A. Immediate spin test
B. Saline method
C. Indirect antiglobulin test
D. Enzyme test
Answer: C. Indirect antiglobulin test
16. Weak D is caused by:
A. Missing D epitopes
B. Reduced antigen expression
C. Absence of D gene
D. ABO incompatibility
Answer: B. Reduced antigen expression
17. Individuals with weak D usually:
A. Produce anti-D
B. Do not produce anti-D
C. Always Rh negative
D. Have Rh-null phenotype
Answer: B. Do not produce anti-D
18. Partial D individuals may produce:
A. Anti-E
B. Anti-c
C. Anti-D
D. Anti-A
Answer: C. Anti-D
19. Partial D occurs due to:
A. Quantitative reduction
B. Hybrid gene formation
C. Gene deletion
D. RhAG mutation
Answer: B. Hybrid gene formation
20. Del phenotype is characterized by:
A. Absence of Rh antigens
B. Very weak D expression
C. Complete D antigen
D. Excess D antigen
Answer: B. Very weak D expression
21. Rh-null phenotype lacks:
A. Only D antigen
B. Only C and E antigens
C. All Rh antigens
D. ABO antigens
Answer: C. All Rh antigens
22. Rh-null individuals commonly show:
A. Polycythemia
B. Leukopenia
C. Hemolytic anemia
D. Thrombocytopenia
Answer: C. Hemolytic anemia
23. Rh-null regulator type is due to mutation in:
A. RHD gene
B. RHCE gene
C. RhAG gene
D. Kell gene
Answer: C. RhAG gene
24. RhAG protein is essential for:
A. ABO expression
B. Rh antigen expression
C. Platelet function
D. Complement activation
Answer: B. Rh antigen expression
25. Rh antigens are fully developed:
A. At 6 months
B. At 1 year
C. At birth
D. After puberty
Answer: C. At birth
26. Rh antigens are absent in:
A. Plasma
B. Saliva
C. Both A and B
D. Serum only
Answer: C. Both A and B
27. Main mechanism of hemolysis in Rh incompatibility is:
A. Intravascular
B. Complement mediated
C. Extravascular
D. Mechanical
Answer: C. Extravascular
28. Rh antibodies can cross placenta because they are:
A. IgM
B. IgA
C. IgE
D. IgG
Answer: D. IgG
29. ABO incompatibility reduces Rh sensitization because:
A. Rh antigens are destroyed early
B. Antibodies neutralize Rh
C. RBCs are cleared rapidly
D. Rh antibodies are IgM
Answer: C. RBCs are cleared rapidly
30. Most effective prevention of Rh immunization is:
A. Blood grouping
B. Cross matching
C. Anti-D immunoglobulin
D. Steroids
Answer: C. Anti-D immunoglobulin
31. Anti-D prophylaxis is given to:
A. Rh-positive mother
B. Rh-negative mother
C. Rh-positive fetus
D. Rh-null mother
Answer: B. Rh-negative mother
32. Rh proteins are primarily involved in transport of:
A. Oxygen
B. Sodium
C. Ammonia and CO₂
D. Glucose
Answer: C. Ammonia and CO₂
33. Absence of Rh proteins leads to:
A. Increased RBC lifespan
B. Membrane instability
C. Thrombosis
D. Leukocytosis
Answer: B. Membrane instability
34. Which Rh antigen is most common after D?
A. E
B. C
C. c
D. e
Answer: C. c
35. Rh system antibodies are best detected by:
A. Slide method
B. Tube saline method
C. Indirect Coombs test
D. Direct Coombs test
Answer: C. Indirect Coombs test
36. Rh antibodies are optimally reactive at:
A. 4°C
B. 22°C
C. 37°C
D. 60°C
Answer: C. 37°C
37. Which condition is most severe in Rh incompatibility?
A. ABO HDN
B. Rh HDN
C. Kell HDN
D. Lewis HDN
Answer: B. Rh HDN
38. Rh antigens do not activate complement efficiently because they are:
A. Carbohydrate
B. Protein antigens
C. Weak antigens
D. IgM mediated
Answer: B. Protein antigens
39. Which test is used to confirm Rh-null phenotype?
A. Slide test
B. Enzyme test
C. Molecular typing
D. Forward grouping
Answer: C. Molecular typing
40. Which Rh antigen variant poses maximum transfusion risk?
A. Weak D
B. Partial D
C. Del
D. Cw
Answer: B. Partial D
41. Rh blood group system consists of more than:
A. 10 antigens
B. 20 antigens
C. 30 antigens
D. 50 antigens
Answer: D. 50 antigens
42. Rh antibodies cause hemolysis mainly in:
A. Liver and spleen
B. Kidney
C. Blood vessels
D. Bone marrow
Answer: A. Liver and spleen
43. Rh antigen expression is restricted to:
A. All body cells
B. Epithelial cells
C. Erythroid cells
D. Platelets
Answer: C. Erythroid cells
44. Weak D differs from partial D because weak D is:
A. Qualitative defect
B. Quantitative defect
C. Complete absence
D. Gene deletion
Answer: B. Quantitative defect
45. Partial D individuals are treated as Rh-negative because they may:
A. Lack RhAG
B. Develop anti-D
C. Be Rh-null
D. Have ABO antibodies
Answer: B. Develop anti-D
46. Rh system inheritance is best described as:
A. Simple dominant
B. Simple recessive
C. Haplotypic inheritance
D. Codominant only
Answer: C. Haplotypic inheritance
47. Rh antibodies are detected during pregnancy by:
A. Forward grouping
B. Reverse grouping
C. Antibody screening
D. Cross match only
Answer: C. Antibody screening
48. Rh antigen density is highest on:
A. Fetal RBCs
B. Newborn RBCs
C. Adult RBCs
D. Reticulocytes
Answer: C. Adult RBCs
49. Rh incompatibility is most likely when mother is:
A. Rh positive
B. Rh negative
C. ABO incompatible
D. Rh-null
Answer: B. Rh negative
50. Rh blood group system is clinically important mainly because of:
A. Frequency
B. Molecular complexity
C. Immunogenicity
D. Secretor status
Answer: C. Immunogenicity