Approach to the patient with Kallmann syndrome

VernacularTitle:卡尔曼综合征的临诊应对
Author: Peipei LI ^{1
,

2} ; Rongmei LU ; Wei LIN ; Huibin HUANG ; Jixing LIANG ; Liantao LI ; Lixiang LIN ; Gang CHEN ; Junping WEN
Author Information

1. 350001 福州,福建医科大学省立临床医学院,福建省立医院内分泌科
2. 福建中医药大学附属福鼎医院
Keywords: Kallmann syndrome; Gene mutation; Neuron migration; Diagnosis; Treatment
From: Chinese Journal of Endocrinology and Metabolism 2018;34(1):72-76
CountryChina
Language:Chinese
Abstract: Kallmann syndrome ( KS) is a rare disease and characteristic of an absence of puberty, infertility, and a defective sensation of smell (anosmia or hyposmia). Here, we analyze the features of a case of KS diagnosed clinically. In addition, the etiology, genetic features, clinical manifestations, diagnosis, and treatment of KS were reviewed.