A new study evaluates a co-designed website aimed at improving resources for congenital hypogonadotropic hypogonadism. This initiative highlights the importance of patient involvement in developing educational tools for rare diseases.
from patients to partners evaluating a co designed website for congenital hypogonadotropic hypogonadism
Original title: “From patients to partners: Evaluating a co-designed website for congenital hypogonadotropic hypogonadism.”