J Pediatr Genet 2023; 12(01): 081-085
DOI: 10.1055/s-0040-1721440
Case Report

Chimerism 47,XY, + 8/46,XX: Follow-up for 11 Years

Acácia Fernandes Lacerda de Carvalho
1   Laboratory of Human Genetics and Mutagenesis, Institute of Biology, Federal University of Bahia, Salvador, Bahia, Brazil
,
Paula Monique Leite Pitanga
1   Laboratory of Human Genetics and Mutagenesis, Institute of Biology, Federal University of Bahia, Salvador, Bahia, Brazil
2   DNA Laboratory – Laboratory Center for Genetics and Molecular Biology, Salvador, Bahia, Brazil
,
Esmeralda Santos Alves
2   DNA Laboratory – Laboratory Center for Genetics and Molecular Biology, Salvador, Bahia, Brazil
3   Department of Medical Genetics, Edgard Santos Teaching Hospital Academic, Federal University of Bahia, Salvador, Bahia, Brazil
,
Diego Santana Chaves Geraldo Miguel
2   DNA Laboratory – Laboratory Center for Genetics and Molecular Biology, Salvador, Bahia, Brazil
,
Laila Damasceno Espirito Santo
1   Laboratory of Human Genetics and Mutagenesis, Institute of Biology, Federal University of Bahia, Salvador, Bahia, Brazil
2   DNA Laboratory – Laboratory Center for Genetics and Molecular Biology, Salvador, Bahia, Brazil
,
Ana Eliete Fernandes de Araújo
1   Laboratory of Human Genetics and Mutagenesis, Institute of Biology, Federal University of Bahia, Salvador, Bahia, Brazil
,
Ana Carolina Pereira Ornellas
2   DNA Laboratory – Laboratory Center for Genetics and Molecular Biology, Salvador, Bahia, Brazil
,
Maria Betânia Pereira Toralles
2   DNA Laboratory – Laboratory Center for Genetics and Molecular Biology, Salvador, Bahia, Brazil
3   Department of Medical Genetics, Edgard Santos Teaching Hospital Academic, Federal University of Bahia, Salvador, Bahia, Brazil
› Author Affiliations

Funding This work was supported by Edgard Santos Teaching Hospital Academic, Federal University of Bahia, Salvador, Bahia, Brazil and by DNA Laboratory – Laboratory Center for Genetics and Molecular Biology, Salvador, Bahia, Brazil.
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Abstract

Approximately 30 sex chromosome discordant chimera cases have been reported to date. In particular, there are few reported cases of chimerism involving coexisting normal and abnormal lineages that each carries a distinct sex chromosome complement. To our knowledge, this is the first case of sexual chimerism with a simultaneous chromosomal aneuploidy involving chromosome 8. This report represents the data from 11 years of follow-up.

Ethical Approval

This study was approved by the Ethics Commission of the Universida de Federal da Bahia and informed written consent was obtained from participating subjects.


Authors' Contributions

A.F.L.C. contributed to the design of the work, genotype–phenotype correlation, and writing the manuscript. D.S.C.G.M. and M.B.P.T. performed the clinical evaluation of the patient and contributed for critical revision and to the final version of the manuscript. P.M.L.P., E.S.A., L.D.E.S., and A.C.P.O. contributed to the analysis and interpretation of the genomic data. A.E.F.A. contributed to the literature review. All authors discussed the results and provided critical feedback to the manuscript.




Publication History

Received: 17 August 2020

Accepted: 16 October 2020

Article published online:
07 December 2020

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