OMICS 放射線学ジャーナル

抽象的な

Kallmann Syndrome: About Two Cases

Soufiane Rostoum, kaoutar Imrani, Meriem Zhim, Sarah Habib Chorfa, Amine Naggar, Nabil Moatassim, Nassar Ittimade

Kallmann syndrome is a rare genetic disorder characterized by hypogonadotropic hypogonadism associated with anosmia or hyposmia. It is a disorder of neuronal migration. Magnetic resonance (MR) imaging is used to visualize the olfactory pathways and to evaluate the olfactory stool. Magnetic resonance (MR) imaging is used to visualize the olfactory tracts and to evaluate the olfactory sulci. We report 2 cases of patients with this syndrome.