PMID- 25016712 OWN - NLM STAT- MEDLINE DCOM- 20140812 LR - 20191112 IS - 1433-6510 (Print) IS - 1433-6510 (Linking) VI - 60 IP - 6 DP - 2014 TI - A case of dispermic chimerism with normal phenotype identified during ABO blood grouping. PG - 1049-54 AB - BACKGROUND: Human chimerism with normal phenotype derived from the fusion of two different zygotes is a rare phenomenon. We describe a case of a phenotypically normal 17-year-old diagnosed with dispermic chimerism during routine ABO blood grouping. METHODS: ABO grouping, ABO genotyping, karyotyping, human leukocyte antigen (HLA) typing, and short tandem repeat (STR) analysis were performed. RESULTS: Forward typing with anti-A and anti-B sera resulted in mixed-field agglutination of red blood cells. The mother and father were blood group O and AB, respectively. The proposita had O1, A201 and B alleles in the ABO locus; O1 was a maternal allele, while A201 and B were the paternal alleles. The proposita karyotype was 46,XX/46,XY. HLA typing revealed that the proposita had three alleles (46, 51, 54) at the HLA-B locus, with the additional allele of paternal origin. STR analysis identified three alleles for five of the 15 markers (D2S1338, TPOX, D8S1179, D19S433, and D21S11) analyzed in the proposita's blood- and skin fibroblast-derived DNA. The additional alleles of TPOX, D8S1179, and D21S11 were of paternal origin. CONCLUSIONS: The genetic findings suggest that this proposita was produced by dispermic fertilization of two identical haploid ova formed by parthenogenetic activation. FAU - Zhu, Pei-Yuan AU - Zhu PY FAU - Yan, Jing-Mei AU - Yan JM FAU - Xue, Min AU - Xue M FAU - Ye, Dong AU - Ye D FAU - Yao, Gen-Hong AU - Yao GH FAU - Luan, Jian-Feng AU - Luan JF LA - eng PT - Case Reports PT - Journal Article PL - Germany TA - Clin Lab JT - Clinical laboratory JID - 9705611 RN - 0 (ABO Blood-Group System) SB - IM MH - ABO Blood-Group System/*blood MH - Adolescent MH - *Blood Grouping and Crossmatching MH - Chimera/*blood MH - Female MH - Humans MH - Microsatellite Repeats MH - Phenotype EDAT- 2014/07/16 06:00 MHDA- 2014/08/13 06:00 CRDT- 2014/07/15 06:00 PHST- 2014/07/15 06:00 [entrez] PHST- 2014/07/16 06:00 [pubmed] PHST- 2014/08/13 06:00 [medline] AID - 10.7754/clin.lab.2013.130401 [doi] PST - ppublish SO - Clin Lab. 2014;60(6):1049-54. doi: 10.7754/clin.lab.2013.130401.