hrp0092p1-275 | Sex Differentiation, Gonads and Gynaecology or Sex Endocrinology (1) | ESPE2019
Ishii Tomohiro
, Hori Naoaki
, Amano Naoko
, Aya Misaki
, Shibata Hirotaka
, Katsumata Noriyuki
, Hasegawa Tomonobu
Background: Lipoid congenital adrenal hyperplasia (LCAH) is caused by mutations in STAR and characterized by defect in adrenal and gonadal steroidogenesis and lipid droplet accumulation in steroidogenic cells. 46,XY patients with classic LCAH typically present with female-type external genitalia, while those with nonclassic LCAH have masculinized external genitalia. The rarity of the nonclassic form precludes the clarification of pubertal and reproduc...