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- W2324623240 abstract "An incidental finding in the blood of a 31 -yr-old Caucasian female was the presence of red cell spherocytosis and stomatocytosis. (Pelger-Huët phenomenon was also present in her neutrophils.) She is symptomatic, with mild splenomegaly and a haemoglobin level of about 11.5 g/dl, with reticulocytosis of 6-10%. The degree of red cell atypia has been quite variable on films taken at different times. Incubated osmotic fragility and autohaemolysis are increased. No immune haemolysis or enzyme defect is demonstrable. Rh phenotyping discloses that the patient has no demonstrable Rh antigens and is thus Rh Null. Serological investigation of the family shows that both parents of the patient have suppressed Rh antigens; the remainder of the family possess varying amounts of Rh antigen including one child who appears to have increased amounts compared with the normal population. The probable genotype of the patient's 3 children is R<sub>1</sub>r while the remainder of the family appears to be R<sub>1</sub>R<sub>1</sub> This family demonstrates the effect of suppressor genes on the expression of Rh antigens and also the quantitative variation of the antigens between members of the family. This and other blood group deletions should be considered in patients with obscure haemolytic anaemia." @default.
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- W2324623240 date "1980-01-01" @default.
- W2324623240 modified "2023-10-16" @default.
- W2324623240 title "A case of Rh Null disease with haemolytic anaemia and pelger-huet anomaly" @default.
- W2324623240 doi "https://doi.org/10.1016/s0031-3025(16)38568-3" @default.
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