Rare Suprasellar Chordoid Meningioma with INI1 Gene Mutation

Background: Chordoid Meningioma is a rare brain tumour characterized genetically by loss of genetic material from chromosome 22q at cytogenetic level resulting in mutation of NF2 gene. Objectives and case report: In the present report, we described a rare case of suprasellar chordoid meningioma,...

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Bibliographic Details
Main Authors: Imad Fadl-Elmula, Rania Giha, Sawsan AH Deaf, Lamyaa Ahmed El Hassan, Ahmed M. Hassan, Mohamed AR Arbab
Format: Article
Language:English
Published: Knowledge E 2017-09-01
Series:Sudan Journal of Medical Sciences
Online Access:https://knepublishing.com/index.php/SJMS/article/view/1001
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