2022
DOI: 10.18502/ijml.v9i3.10902
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Identification of First Patient With Rh Null Phenotype in Southeast Iran

Abstract: Background and Aims: Rhnull, with an estimated incidence of one per 6,000,000 individuals, is an extremely rare disorder with an autosomal recessive pattern of inheritance that is more common in societies with a high rate of consanguinity. Materials and Methods: In this study, we report the first case with Rhnull, a blood group phenotype in southeast Iran, which was diagnosed during pretransfusion testing. Results and Conclusions: A 21-year-old woman with a positive parents' consanguineous marriage… Show more

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