hrp0098p2-264 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2024

Bilateral cryptorchidism: should be systematically explored?

Bergougnoux Anne , Tessier Benoit , Gaspari Laura , Servant Nadege , Cazals Aurelie , Pierre Guibal Marie , Kalfa Nicolas , Paris Françoise

Background: Currently, 1-4% of newborns have cryptorchidism and 30% of them have bilateral cryptorchidism (BC). BC should rule out 46, XX Disorder of Sexual Development (DSD). In 46, XY patients gonosomal abnormalities, alterations in genes involved in 46, XY DSD or hypogonadotropic hypogonadism may be the cause. Currently, patients with BC undergo early orchiopexy in the first 18 months of life. However, in these patients, BC etiology, pubertal development an...