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kaoutar Imrani
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Kallmann Syndrome: About Two Cases
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 t... Read More»
Soufiane Rostoum, kaoutar Imrani, Meriem Zhim, Sarah Habib Chorfa, Amine Naggar, Nabil Moatassim and Nassar Ittimade
: OMICS J Radiol 2023, 12:475
10.4172/2167-7964.1000475Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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