Other genes involved in KS remain to be discovered as mutations in the genes identified so far are detected in less than 30% of the patients.
[baillement.com]
hypogonadotrope (4) Syndrome de Cushing Hypothyroïdie Hypopituitarisme Hyperprolactinémie Décrire : Syndrome de Kallmann Hypogonadisme Hypogonadotrope Syndrome de Kallmann
[brainscape.com]
To date, five causative genes have been identified: KAL1 (Xp22.3), responsible for the X-linked form, and FGFR1 (8p12) FGF8 (10q24), PROKR2 (20p13), and PROK2 (3p21.1), which
[baillement.com]