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Isolated hypogonadotropic hypogonadism , also called idiopathic or congenital hypogonadotropic hypogonadism , as well as isolated or congenital gonadotropin-releasing hormone deficiency , is a condition which results in a small subset of cases of hypogonadotropic hypogonadism due to deficiency in or insensitivity to gonadotropin-releasing hormone where the function and anatomy of the anterior pituitary is otherwise normal and secondary causes of HH are not present.
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