Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of cases Vanessa Brito Campoy Rocha, Gil Guerra-Júnior,

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Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of cases Vanessa Brito Campoy Rocha, Gil Guerra-Júnior, M.D., Ph.D., Antonia Paula Marques-de-Faria, M.D., Ph.D., Maricilda Palandi de Mello, Ph.D., Andréa Trevas Maciel-Guerra, M.D., Ph.D. Fertility and Sterility Volume 96, Issue 6, Pages 1431-1434 (December 2011) DOI: 10.1016/j.fertnstert.2011.09.009 Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions

Figure 1 Pedigrees of nine families with complete gonadal dysgenesis (CGD) and parental consanguinity. (A–G) 46,XX CGD; (H and I) 46,XY CGD (cases 7 and 8, respectively—see Table 1). Solid circles represent individuals with complete gonadal dysgenesis and female phenotype, and the square containing a solid circle represents an individual with sex ambiguity who was raised as a girl. Fertility and Sterility 2011 96, 1431-1434DOI: (10.1016/j.fertnstert.2011.09.009) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions