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...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Knowledge E
2017-04-01
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Series: | Sudan Journal of Medical Sciences |
Subjects: | |
Online Access: | https://doi.org/10.18502/sjms.v12i3.1001 |