Browsing Centre for Endocrinology by Subject "Kallmann syndrome"
Now showing items 1-3 of 3
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Gonadotropins for pubertal induction in males with hypogonadotropic hypogonadism: systematic review and meta-analysis.
(2024-01-03)OBJECTIVE: Hypogonadotropic hypogonadism is characterized by inadequate secretion of pituitary gonadotropins, leading to absent, partial, or arrested puberty. In males, classical treatment with testosterone promotes ... -
Outcomes and experiences of adults with congenital hypogonadism can inform improvements in the management of delayed puberty.
(2024-01-29)Patients with congenital hypogonadism will encounter many health care professionals during their lives managing their health needs; from antenatal and infantile periods, through childhood and adolescence, into adult life ...