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

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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Bibliographic Details
Main Author: HE Qinyu, WANG Wei, CHEN Lifen, ZHANG Xuelei, DONG Zhiya
Format: Article
Language:zho
Published: Editorial Office of Journal of Diagnostics Concepts & Practice 2022-10-01
Series:Zhenduanxue lilun yu shijian
Subjects:
|familial male precocious puberty|luteinizing hormone/choriogonadotropin receptor gene|functional acquired mutation|etiology diagnosis
Online Access:https://www.qk.sjtu.edu.cn/jdcp/fileup/1671-2870/PDF/1674993692273-1367038869.pdf

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https://www.qk.sjtu.edu.cn/jdcp/fileup/1671-2870/PDF/1674993692273-1367038869.pdf

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