Resumo:
x development caused by mutations in genes located in the Y chromosome. It’s
typically described in female individuals with a 46XY karyotype and streak gonads, and it’s
normally diagnosed in adolescence because of the absence of menstruation, with or without
the spontaneous female sexual development. Given the physical, pshychological and social
aspects of this disease, it’s important to discuss about the different clinical presentations in
order to achieve an earlier diagnosis and therefore an effective treatment, which could prevent
more serious complications. Considering the importance of the subject, this study aimed to
describe three different cases of Swyer Syndrome, all being followed up at the gynecology
outpatient clinic of the Unidade de Saúde da Mulher at the Complexo Hospitalar Universitário
Professor Edgard Santos (C-HUPES). It includes three cases reports and a narrative review of
the literature on the reported topic
