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, whi...

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Bibliographic Details
Main Authors: Imad Fadl-Elmula, Rania Giha, Sawsan A. H. Deaf, Lamyaa Ahmed El Hassan, Ahmed M. Hassan, Mohamed A. R. Arbab
Format: Article
Language:English
Published: Knowledge E 2017-04-01
Series:Sudan Journal of Medical Sciences
Subjects:
Online Access:https://doi.org/10.18502/sjms.v12i3.1001