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Revista Med
versión impresa ISSN 0121-5256versión On-line ISSN 1909-7700
Resumen
SALGADO, Perla Cristina et al. Clinical and Cytogenetic Analysis of a Case of SRY-Negative XX Testicular Disorder of Sex Development. Rev. Med [online]. 2019, vol.27, n.1, pp.45-52. Epub 26-Nov-2022. ISSN 0121-5256. https://doi.org/10.18359/rmed.4753.
XX testicular disorder of sex development (DSD) is a pathology that occurs in an individual with a 46,XX karyotype and an anatomical phenotype of male external genitalia, which may vary from normal to ambiguous. Clinically, two subgroups of SRY-negative and SRY-positive, 46, XX men have been described, depending on the presence of the SRY gene that is normally found on the Y chromosome participating in testicular determination. This article describes the personal history and clinical findings of an infant with urethral meatus abnormalities in whom a 46,XX chromosome set was identified. Also, fluorescent in situ hybridization was performed in peripheral blood lymphocytes which demonstrated the absence of the SRY gene and confirmed the presence of two X chromosomes.
Palabras clave : 46,XX testicular disorder of sex development; 46,XX male; SRY-negative; fluorescent in situ hybridization.