“…However, it was similar to the 67% found in a more recent study (20), in which the sample was also formed only by patients with the complete form of the disease based on physical, endocrinological, surgical, and histopathological examinations. Those authors suggested that some patients classified as having ''gonadal dysgenesis'' in some previous reports may in fact have had the incomplete form or some other sex-reversal disorder characterized by female external genitalia and 46,XY karyotype (20). In addition, it must be considered that recent advances in the field of molecular genetics have allowed a more accurate analysis of the SRY gene.…”