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Blood Diathesis in a Patient of Rare Blood Group 'Bombay Phenotype'
被引:3
|作者:
Awan, Sara A.
[1
]
Junaid, Ayesha
[2
]
Khan, Samreen
[1
]
Jahangir, Sehreen
[3
]
机构:
[1] Shifa Int Hosp, Dept Hematol, Islamabad, Pakistan
[2] Shifa Int Hosp, Hematol, Islamabad, Pakistan
[3] Shifa Internal Hosp, Dept Hematol, Islamabad, Pakistan
来源:
关键词:
von willebrand disease;
bombay phenotype;
blood transfusion;
von willebrand factor;
abo blood group;
von willebrand antigen;
D O I:
10.7759/cureus.3488
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
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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