2020•Sexual DevelopmentRequires access
Association between Down Syndrome and Disorders of Sex Development: Report of Three Cases and Review of 188 Cases in the Literature
Octavio O. Santos-Neto, Marina H. Mariano, Antonia Paula Marques‐de‐Faria, Juliana Gabriel Ribeiro de Andrade, Társis Paiva Vieira, Nilma L. Viguetti‐Campos, Ana Paula Santos, Maricilda Palandi de Mello, Taís Nitsch Mazzola, Mara Sanches Guaragna, Helena Fabbri‐Scallet, Durval Damiani, Leandra Steinmetz, Marianna R. Ferreira, Paula A. Saito, Jean C. Sievert, Andréa Trevas Maciel‐Guerra, Gil Guerra‐Júnior
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Abstract
In this study, we present 3 cases of Down syndrome (DS) associated with disorders/differences of sex development (DSD) and review the literature on this topic. Case 1: 1-year-old child with male genitalia and DS phenotype, 47,XX,+21 karyotype and testicular DSD. Case 2: 11-month-old child with male genitalia and few DS dysmorphisms, 45,X/47,XY,+21 karyotype, and mixed gonadal dysgenesis. Case 3: 4-month-old child with female genitalia and DS phenotype, 47,XY,+21 karyotype and XY complete gonadal dysgenesis. In the literature, among 188 patients, 107 (57%) had Klinefelter syndrome and 61 (33%) Turner syndrome, 12 (6%) had mixed gonadal dysgenesis, 2 (1%) had partial androgen insensitivity, 2 (1%) ovotesticular DSD, and the others had congenital adrenal hyperplasia, XY partial gonadal dysgenesis, XY complete gonadal dysgenesis, and complete androgen insensitivity (1 case each). A typical DS phenotype was found in all individuals of the revision, with the exception of one case, but DSD features were not always reported. In conclusion, the association of DS with sex chromosome DSD is the most frequently observed, whereas associations with 46,XX and 46,XY DSD is extremely rare.