ISSN:2167-7964

Journal of Radiology
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  • Case Report   
  • OMICS J Radiol 2023, Vol 12(8): 475
  • DOI: 10.4172/2167-7964.1000475

Kallmann Syndrome: About Two Cases

Soufiane Rostoum*, Kaoutar Imrani, Meriem Zhim, Sarah Habib Chorfa, Amine Naggar, Nabil Moatassim and Nassar Ittimade
Department of Central Radiology, Ibn Sina University Hospital Center, Rabat, Morocco
*Corresponding Author : Soufiane Rostoum, Department of Central Radiology, Ibn Sina University Hospital Center, Rabat, Morocco, Email: rostoum.soufiane@gmail.com

Received Date: Aug 05, 2023 / Published Date: Aug 31, 2023

Abstract

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.

Citation: Rostoum S, Imrani K, Zhim M, Chorfa SH, Naggar A (2023) KallmannSyndrome: About Two Cases. OMICS J Radiol 12: 475. Doi: 10.4172/2167-7964.1000475

Copyright: © 2023 Rostoum S, et al. This is an open-access article distributedunder the terms of the Creative Commons Attribution License, which permitsunrestricted use, distribution, and reproduction in any medium, provided theoriginal author and source are credited.

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