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Weak D types 38 and 11: determination of frequencies in a Brazilian population and validation of an easy molecular assay for detection


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Westhoff CM. The Rh blood group system in review: a new face for the next decade. Transfusion 2004;44:1663–73. Westhoff CM. The Rh blood group system in review: a new face for the next decade . Transfusion 2004 ; 44 : 1663 73 . 10.1111/j.0041-1132.2004.04237.x15504174 Search in Google Scholar

Flegel WA. Molecular genetics and clinical applications for RH. Transfus Apher Sci 2011;44:81–91. Flegel WA. Molecular genetics and clinical applications for RH . Transfus Apher Sci 2011 ; 44 : 81 91 . 10.1016/j.transci.2010.12.013304251121277262 Search in Google Scholar

Wagner FF, Flegel WA. The rhesus site. Transfus Med Hemother 2014;41:357–63. Wagner FF Flegel WA. The rhesus site . Transfus Med Hemother 2014 ; 41 : 357 63 . 10.1159/000366176426449225538538 Search in Google Scholar

Westhoff CM. Rh complexities: serology and DNA genotyping. Transfusion 2007;47:17S–22S. Westhoff CM. Rh complexities: serology and DNA genotyping . Transfusion 2007 ; 47 : 17S 22S . 10.1111/j.1537-2995.2007.01305.x17593281 Search in Google Scholar

Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood 1999; 93:385–93. Wagner FF Gassner C Muller TH Schonitzer D Schunter F Flegel WA. Molecular basis of weak D phenotypes . Blood 1999 ; 93 : 385 93 . 10.1182/blood.V93.1.385 Search in Google Scholar

Sandler SG, Chen LN, Flegel WA. Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype. Br J Haematol 2017;179:10–9. Sandler SG Chen LN Flegel WA. Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype . Br J Haematol 2017 ; 179 : 10 9 . 10.1111/bjh.14757561284728508413 Search in Google Scholar

Muller TH, Wagner FF, Trockenbacher A, et al. PCR screening for common weak D types shows different distributions in three Central European populations. Transfusion 2001;41: 45–52. Muller TH Wagner FF Trockenbacher A , PCR screening for common weak D types shows different distributions in three Central European populations . Transfusion 2001 ; 41 : 45 52 . 10.1046/j.1537-2995.2001.41010045.x11161244 Search in Google Scholar

Reid ME, Halter Hipsky C, Hue-Roye K, Hoppe C. Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease. Blood Cells Mol Dis 2014;52:195–202. Reid ME Halter Hipsky C Hue-Roye K Hoppe C. Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease . Blood Cells Mol Dis 2014 ; 52 : 195 202 . 10.1016/j.bcmd.2013.11.003395444324309423 Search in Google Scholar

Wagner FF, Frohmajer A, Ladewig B, et al. Weak D alleles express distinct phenotypes. Blood 2000;95:2699–708. Wagner FF Frohmajer A Ladewig B , Weak D alleles express distinct phenotypes . Blood 2000 ; 95 : 2699 708 . 10.1182/blood.V95.8.2699 Search in Google Scholar

Noizat-Pirenne F, Tournamille C. Relevance of RH variants in transfusion of sickle cell patients. Transfus Clin Biol 2011;18:527–35. Noizat-Pirenne F Tournamille C. Relevance of RH variants in transfusion of sickle cell patients . Transfus Clin Biol 2011 ; 18 : 527 35 . 10.1016/j.tracli.2011.09.00122024128 Search in Google Scholar

Dezan MR, Oliveira VB, Gomes CN, et al. High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype. J Clin Lab Anal 2018;32:e22596. Dezan MR Oliveira VB Gomes CN , High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype . J Clin Lab Anal 2018 ; 32 : e22596 . 10.1002/jcla.22596 Search in Google Scholar

Costa S, Martin F, Chiba A, Langhi D Jr, Chiattone C, Bordin J. RHD alleles and D antigen density among serologically D–C+ Brazilian blood donors. Transfus Med 2014;24:60–1. Costa S Martin F Chiba A Langhi D Jr Chiattone C Bordin J. RHD alleles and D antigen density among serologically D–C+ Brazilian blood donors . Transfus Med 2014 ; 24 : 60 1 . 10.1111/tme.12088 Search in Google Scholar

Maaskant-van Wijk PA, Faas BH, de Ruijter JA, et al. Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons. Transfusion 1998;38:1015–21. Maaskant-van Wijk PA Faas BH de Ruijter JA , Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons . Transfusion 1998 ; 38 : 1015 21 . 10.1046/j.1537-2995.1998.38111299056309.x Search in Google Scholar

Tax MG, van der Schoot CE, van Doorn R, Douglas-Berger L, van Rhenen DJ, Maaskant-van Wijk PA. RHC and RHc genotyping in different ethnic groups. Transfusion 2002; 42:634–44. Tax MG van der Schoot CE van Doorn R Douglas-Berger L van Rhenen DJ Maaskant-van Wijk PA. RHC and RHc genotyping in different ethnic groups . Transfusion 2002 ; 42 : 634 44 . 10.1046/j.1537-2995.2002.00096.x Search in Google Scholar

Singleton BK, Green CA, Avent ND, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype. Blood 2000;95:12–8. Singleton BK Green CA Avent ND , The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype . Blood 2000 ; 95 : 12 8 . 10.1182/blood.V95.1.12 Search in Google Scholar

Wagner FF, Gassner C, Muller TH, Schonitzer D, Schunter F, Flegel WA. Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features. Blood 1998;91:2157–68. Wagner FF Gassner C Muller TH Schonitzer D Schunter F Flegel WA. Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features . Blood 1998 ; 91 : 2157 68 . 10.1182/blood.V91.6.2157 Search in Google Scholar

Chiu RW, Murphy MF, Fidler C, Zee BC, Wainscoat JS, Lo YM. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clin Chem 2001;47:667–72. Chiu RW Murphy MF Fidler C Zee BC Wainscoat JS Lo YM. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach . Clin Chem 2001 ; 47 : 667 72 . 10.1093/clinchem/47.4.667 Search in Google Scholar

Perco P, Shao CP, Mayr WR, Panzer S, Legler TJ. Testing for the D zygosity with three different methods revealed altered Rhesus boxes and a new weak D type. Transfusion 2003;43:335–9. Perco P Shao CP Mayr WR Panzer S Legler TJ. Testing for the D zygosity with three different methods revealed altered Rhesus boxes and a new weak D type . Transfusion 2003 ; 43 : 335 9 . 10.1046/j.1537-2995.2003.00313.x Search in Google Scholar

Flegel WA, Curin-Serbec V, Delamaire M, et al. Section 1B: Rh flow cytometry. Coordinator’s report. Rhesus index and antigen density: an analysis of the reproducibility of flow cytometric determination. Transfus Clin Biol 2002;9:33–42. Flegel WA Curin-Serbec V Delamaire M , Section 1B: Rh flow cytometry. Coordinator’s report. Rhesus index and antigen density: an analysis of the reproducibility of flow cytometric determination . Transfus Clin Biol 2002 ; 9 : 33 42 . 10.1016/S1246-7820(01)00213-0 Search in Google Scholar

Arnoni CP, Latini FR, Muniz JG, et al. A simple approach to screen rare donors in Brazil. Immunohematology 2015;31: 20–3. Arnoni CP Latini FR Muniz JG , A simple approach to screen rare donors in Brazil . Immunohematology 2015 ; 31 : 20 3 . 10.21307/immunohematology-2019-066 Search in Google Scholar

Costa SS, Chiba A, Cruz B, Langhi Júnior D, Bordin JO. RHD*weak D type 38: a family study. Rev Bras Hematol Hemoter 2016;38:79–81. Costa SS Chiba A Cruz B Langhi Júnior D Bordin JO. RHD*weak D type 38: a family study . Rev Bras Hematol Hemoter 2016 ; 38 : 79 81 . 10.1016/j.bjhh.2015.10.001478676326969778 Search in Google Scholar

Ansart-Pirenne H, Asso-Bonnet M, Le Pennec PY, Roussel M, Patereau C, Noizat-Pirenne F. RhD variants in Caucasians: consequences for checking clinically relevant alleles. Transfusion 2004;44:1282–6. Ansart-Pirenne H Asso-Bonnet M Le Pennec PY Roussel M Patereau C Noizat-Pirenne F. RhD variants in Caucasians: consequences for checking clinically relevant alleles . Transfusion 2004 ; 44 : 1282 6 . 10.1111/j.1537-2995.2004.04063.x15318849 Search in Google Scholar

Dogic V, Bingulac-Popovic J, Babic I, et al. Distribution of weak D types in the Croatian population. Transfus Med 2011;21:278–9. Dogic V Bingulac-Popovic J Babic I , Distribution of weak D types in the Croatian population . Transfus Med 2011 ; 21 : 278 9 . 10.1111/j.1365-3148.2011.01071.x21269342 Search in Google Scholar

Wagner FF, Frohmajer A, Flegel WA. RHD positive haplotypes in D negative Europeans. BMC Genet 2001;2:10. Wagner FF Frohmajer A Flegel WA. RHD positive haplotypes in D negative Europeans . BMC Genet 2001 ; 2 : 10 . 10.1186/1471-2156-2-103726711495631 Search in Google Scholar

Araujo F, Rodrigues MJ, Monteiro F, et al. Weak D type 2 is the most prevalent weak D type in Portugal. Transfus Med 2006;16:63–7. Araujo F Rodrigues MJ Monteiro F , Weak D type 2 is the most prevalent weak D type in Portugal . Transfus Med 2006 ; 16 : 63 7 . 10.1111/j.1365-3148.2005.00638.x16480441 Search in Google Scholar

Rodrigues M, Rodrigues F, Tilley L, Poole J, Chabert T, Sousa G. Several new examples of weak D type 38 in the Portuguese population [abstract]. Transfusion 2006;46(Suppl):141A–2. Rodrigues M Rodrigues F Tilley L Poole J Chabert T Sousa G. Several new examples of weak D type 38 in the Portuguese population [abstract] . Transfusion 2006 ; 46 (Suppl) : 141A 2 . Search in Google Scholar

Ouchari M, Romdhane H, Chakroun T, et al. Weak D in the Tunisian population. Blood Transfus 2015;13:295–301. Ouchari M Romdhane H Chakroun T , Weak D in the Tunisian population . Blood Transfus 2015 ; 13 : 295 301 . Search in Google Scholar

Dinardo CL, Kelly S, Dezan MR, et al. Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies. Transfusion 2019;59: 3228–35. Dinardo CL Kelly S Dezan MR , Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies . Transfusion 2019 ; 59 : 3228 35 . 10.1111/trf.15479678537031408202 Search in Google Scholar

eISSN:
1930-3955
Sprache:
Englisch
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4 Hefte pro Jahr
Fachgebiete der Zeitschrift:
Medizin, Klinische Medizin, Laboratoriumsmedizin