Diagnosis and treatment of familial male precocious puberty caused by LHCGR gene mutation: two case reports and literature review

Objective: To report the clinical features, gene detection results and treatment results of two patients with familial male limited precocious puberty(FMPP). Methods: Detailed medical history collection and physical examination were carried out in 2 FMPP patients. LHRH challenge test, sex hormone, a...

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Manylion Llyfryddiaeth

Prif Awdur:	HE Qinyu, WANG Wei, CHEN Lifen, ZHANG Xuelei, DONG Zhiya
Fformat:	Artigo
Iaith:	Chinês
Cyhoeddwyd:	Editorial Office of Journal of Diagnostics Concepts & Practice 2022-10-01
Cyfres:	Zhenduanxue lilun yu shijian
Pynciau:	|familial male precocious puberty|luteinizing hormone/choriogonadotropin receptor gene|functional acquired mutation|etiology diagnosis
Mynediad Ar-lein:	https://www.qk.sjtu.edu.cn/jdcp/fileup/1671-2870/PDF/1674993692273-1367038869.pdf
Tagiau:	Ychwanegu Tag Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!