Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review

• Główni autorzy: Jihyun Ha (Autor), Yunha Choi (Autor), Mo Kyung Jung (Autor), Eun-Gyong Yoo (Autor), Han-Wook Yoo (Autor)
• Format: Książka
• Wydane: Korean Society of Pediatric Endocrinology, 2024-02-01T00:00:00Z.
• Hasła przedmiotowe: article
• Dostęp online: Connect to this object online.

Familial male-limited precocious puberty (FMPP) is a rare form of gonadotropin-independent precocious puberty that is caused by an activating mutation of the LHCGR gene. Herein, we report a case of FMPP with a mutation of the LHCGR gene in a Korean boy with familial history of precocious puberty thr...