Blood Diathesis in a Patient of Rare Blood Group 'Bombay Phenotype'
Bombay blood group or Oh phenotype is a rare autosomal recessive phenotype within the ABO blood grouping system. It occurs due to a mutation in the H gene that produces H antigen on red blood cells (RBCs). Individuals with two mutant H genes lack H antigen on RBCs and have anti-H antibodies in serum...
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Veröffentlicht in: | Curēus (Palo Alto, CA) CA), 2018-10, Vol.10 (10), p.e3488 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Bombay blood group or Oh phenotype is a rare autosomal recessive phenotype within the ABO blood grouping system. It occurs due to a mutation in the H gene that produces H antigen on red blood cells (RBCs). Individuals with two mutant H genes lack H antigen on RBCs and have anti-H antibodies in serum. At the time of blood grouping, this blood group mimics O blood group but it shows incompatibility with O group blood during cross matching. Several studies have reported an association of decreased von Willebrand factor (VWF) levels in plasma with ABO blood groups. Here we report a case of a 19-year-old male, who was labelled as Bombay phenotype and later found to have markedly reduced plasma VWF levels. |
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ISSN: | 2168-8184 2168-8184 |
DOI: | 10.7759/cureus.3488 |