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      A Dispermic Chimera with Mixed Field Blood Group B and Mosaic 46,XY/47,XYY Karyotype

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          Abstract

          Chimerism in humans is a rare phenomenon often initially identified in the resolution of an ABO blood type discrepancy. We report a dispermic chimera who presented with mixed field in his B antigen typing that might have been mistaken for the B 3 subtype. The propositus is a healthy Korean male blood donor. Neither his clinical history nor initial molecular investigation of his ABO gene explained his mixed field agglutination with murine anti-B. Chimerism was suspected, and 9 short tandem repeat (STR) loci were analyzed on DNA extracted from blood, buccal swabs, and hair from this donor and on DNA isolated from peripheral blood lymphocytes from his parents. The propositus' red blood cells demonstrated mixed field agglutination with anti-B. Exon 6 and 7 and flanking intronic regions of his ABO gene were sequenced and revealed an O01/O02 genotype. B allele haplotype-specific PCR, along with exon 6 and 7 cloning and sequencing demonstrated a third ABO allele, B101. Four STR loci demonstrated a pattern consistent with a double paternal chromosome contribution in the propositus, thus confirming chimerism. His karyotype revealed a mosaic pattern: 32/50 metaphases were 46,XY and 18/50 metaphases demonstrated 47,XYY.

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          Human Blood Groups

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            Blood group chimerism in human multiple births is not rare.

            Twin blood group chimerism seems to be very rare in humans. The 30-40 previously reported cases usually were found by mere coincidence during routine blood grouping in hospitals or blood banks. Usually in these cases frank blood group mixtures of, for example, 50/50%, 25/75%, or 5/95% at most were seen. Smaller percentages are very difficult to notice during routine work-up. Using a sensitive fluorescence technique (sensitivity > 0.01%) we detected blood group chimerism in 32/415 (8%) twin pairs and 12/57 (21%) triplet pairs, respectively, which is a higher incidence than reported previously.
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              A human parthenogenetic chimaera.

              In mice, parthenogenetic embryos die at the early postimplantation stage as a result of developmental requirements for paternally imprinted genes, particularly for formation of extraembryonic tissues. Chimaeric parthenogenetic normal mice are viable, however, due to non-random differences in distribution of their two cell types. Species differences in imprinting patterns in embryo and extra-embryonic tissues mean that there are uncertainties in extrapolating these experimental studies to humans. Here, however, we demonstrate that parthenogenetic chimaerism can indeed result in viable human offspring, and suggest possible mechanisms of origin for this presumably rare event.
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                Author and article information

                Journal
                J Korean Med Sci
                JKMS
                Journal of Korean Medical Science
                The Korean Academy of Medical Sciences
                1011-8934
                1598-6357
                June 2007
                30 June 2007
                : 22
                : 3
                : 553-556
                Affiliations
                Department of Laboratory Medicine, Chonnam National University Hospital & Medical School, Gwangju, Korea.
                [* ]The Institute for Transfusion Medicine and Department of Pathology, University of Pittsburgh, Pittsburgh, U.S.A.
                []Gwangju-Chonnam Red Cross Blood Center, Gwangju, Korea.
                []Department of Forensic Medicine, Chonnam National Medical School, Gwangju, Korea.
                Author notes
                Address for correspondence: Dong Wook Ryang, M.D. Department of Laboratory Medicine, Chonnam National University Medical School, 8 Hark-dong, Dong-gu, Gwangju 501-757, Korea. Tel: +82.62-220-5340, Fax: +82.62-224-2518, dwryang@ 123456chonnam.ac.kr
                Article
                10.3346/jkms.2007.22.3.553
                2693654
                17596670
                a43a4758-f1d7-4b95-bee7-09e5ee9913c5
                Copyright © 2007 The Korean Academy of Medical Sciences

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 October 2005
                : 02 February 2006
                Categories
                Case Report

                Medicine
                abo blood type,chimerism,xyy karyotype,mosaicism
                Medicine
                abo blood type, chimerism, xyy karyotype, mosaicism

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