Zaghouani Houneida, Slim Ines, Zina Neila Ben, Mallat Najoua, Tajouri Houda, Kraiem Chakib
Department of Radiology, Farhat Hached University Hospital, Sousse, Tunisia.
Indian J Endocrinol Metab. 2013 Oct;17(Suppl 1):S142-5. doi: 10.4103/2230-8210.119536.
Kallmann syndrome (KS) is a disease clinically characterized by the association of hypogonadotrophic hypogonadism and anosmia or hyposmia. It is a neuronal migration disorder. Magnetic resonance (MR) imaging is used to visualize the olfactory tracts and to evaluate the olfactory sulci. Five patients who clinically had hypogonadotrophic hypogonadism were examined by MR. Thin coronal images of the interior frontal region were used to determine presence or absence of olfactory tract and to evaluate the olfactory sulci.
卡尔曼综合征(KS)是一种临床上以低促性腺激素性性腺功能减退与嗅觉缺失或嗅觉减退相关为特征的疾病。它是一种神经元迁移障碍性疾病。磁共振(MR)成像用于显示嗅束并评估嗅沟。对5例临床上患有低促性腺激素性性腺功能减退的患者进行了MR检查。使用额叶内部的薄层冠状位图像来确定嗅束的有无并评估嗅沟。