It has been a common and reasonable presumption that the association of unusual shortness of stature and retarded genital development bespeaks hypopituitarism, especially in the absence of cretinism, gross malnutrition or systemic disease. Even when roentgenological examination of the skull and studies of the visual fields are normal this presumption persists, fortified by a wealth of physiological data establishing the hypophysis as a controlling agent both for growth and for gonadal function and by our knowledge that demonstrable destructive pituitary disease produces similar physical consequences. Low titers of urinary gonadotropins would be expected in such people. However four short girls with deficient sexual development excreted 200 to 500 mouse units of gonadotropins per day, as judged by induced estrin production in the immature mouse, values corresponding to those of the castrate and usually taken to suggest primary ovarian insufficiency. Coincidentally, Albright, Smith and Fraser (1) have had a...