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