Recurrent bacteriuria and primary biliary cirrhosis: ABO blood group, P1 blood group, and secretor status.
نویسندگان
چکیده
منابع مشابه
Recurrent bacteriuria and primary biliary cirrhosis: ABO blood group, P1 blood group, and secretor status.
Patients with primary biliary cirrhosis have an abnormally high incidence of urinary tract infection (35%). Susceptibility to urinary infection and other infectious diseases has been linked with certain blood group antigens and secretor status. We have therefore studied these characteristics in patients with primary biliary cirrhosis. We were unable to show any abnormal distribution in blood gr...
متن کاملABO blood group, secretor state, and susceptibility to recurrent urinary tract infection in women.
ABO blood group and secretor state was determined in 319 women with recurrent urinary tract infection and compared with those of a control group of 334 women of similar age ranges. Women of blood groups B and AB who are non-secretors of blood group substances showed a significant relative risk of recurrent urinary tract infection of 3.12 (95% confidence limits, 1.49 and 6.52) in comparison with...
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Significant bacteriuria was found in 19% of 87 women with primary biliary cirrhosis, whereas in 89 women with other types of chronic liver disease bacteriuria was present in only 7%. In 74 women with rheumatoid arthritis 8% were bacteriuric. Midstream urine specimens obtained from 144 consecutive women with primary biliary cirrhosis attending hospital over a two year period showed that 50 (35%)...
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The current study was carried out on 550 healthy population having 250 males and 300 females. Five ml venousblood was collected following standard biosafety measures. ABO blood grouping was done by Tile method and found blood group B dominant in both sexes i.e 180 male and 120 female were found with blood group B. Moreover, 2 ml of saliva was also collected from allvolunteers. Secretor status w...
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Acute lymphoblastic leukemia (ALL) constitute a family of genetically heterogeneous lymphoid neoplasms derived from B- and T-lymphoid progenitors. ALL affects both children and adults. Diagnosis is based on morphologic, immunophenotypic, and genetic features that allow differentiation from normal progenitors and other hematopoietic and nonhematopoietic neoplasms. The aim of this study was to in...
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ژورنال
عنوان ژورنال: Journal of Clinical Pathology
سال: 1984
ISSN: 0021-9746
DOI: 10.1136/jcp.37.9.1055