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Feminizing genitoplasty (FGP) involves modification of a hypertrophic clitoris, vaginoplasty, and modelling of the labia. FGP is performed during childhood and usually in one stage. In 1996-1999 30 patients with intersex were operated on. 25 girls with female pseudohermaphroditism caused by congenital adrenal hyperplasia (CAH), 3 patients with mixed gonadal dysgenesis (MGD), 1 patient with male pseudohermaphroditism and one female patient with true hermaphroditism (HFV). Seventeen patients were between the ages of 3 and 6 years, 13 patients (all female with CAH) were 13 to 21 years old. One-stage FGP, i.e. partial resection of the clitoris and vaginoplasty (VP) was performed in 11 patients. A two-stage operation, i.e. partial resection of the clitoris and subsequent vaginoplasty, was done in 3 patients (all with VHN with a high-orifice vagina). Vaginoplasty after excision of the clitoris was made in 13 patients (all with CAH, 5 of them with a high-orifice vagina). Three female patients (2 VHN, 1 HFV) had partial resection of the clitoris and wait to have VP. Fourteen patients with partial resection of the clitoris healed p.p. Healing p.s. was recorded in 5/27 patients with vaginoplasty (all CAH). Three of them were older, menstruating and obese. In 4/14 patients after partial resection of the clitoris both modelling and fixation of the glans clitoridis was necessary. Urinary incontinence was not recorded. Stricture of the vaginal orifice was found in one 6-year-old patient with CAH after reconstruction of a high-orifice vagina. Thirteen older patients have a normal vaginal orifice, two of them have sexual intercourse. FGP can be performed already at toddler age, the cosmetic effect is favourable, the glans clitoridis is preserved and the psychosexual development of patients is not impaired. FGP can be used also in adults, severely virilized patients.

A stepwise resolution of the role of individual genes known to play role in sex determination is presented. Cytogenetic abnormalities e.g. male phenotype with XX and female phenotype with XY gonosomal complements helped substantially to ascertain SRY (Sex region of Y) gene activity to be essential for sex phenotype development control. This control seems to be rather suppressive than activating.

The concentration of testosterone in the blood and its response to administration of chorionic gonadotropin was examined in two bovine intersexes (testicular pseudo-hermaphroditism) and two control bulls without disorders in sexual differentiation. The levels of testosterone in the blood were markedly lower in both intersexes than in the control bulls. Both intersexes, unlike the control bulls, also showed a response of the blood testosterone level to the administration of chorionic gonadotropin. The conclusion is that in the given type of intersexuality the incretion function of the testes is mardedly deficient as to androgen production and functional hormonal reserve.

Gonads were studied from 11 phenotypical women with syndromes of abnormal sexual differentiation. The group comprised 4 cases of complete and 3 cases of uncomplete testicular feminization one masculine pseudohermaphrodite with mosaic 45,XO/46,XY and 3 cases of Swyer syndrome. Sertoli-cells-only tubules with some nodes of so called "tubular adenomas" were the prevailing finding. One classical seminoma and two carcinomas in situ were registered in dysgenetic gonads.