Volume 2, Issue 5 (Spring 2016)                   Caspian.J.Neurol.Sci 2016, 2(5): 50-53 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Ghabeli-Juibary A, Rezaeitalab F. Neuroacanthocytosis in Two Brothers: An Ultra-rare Cause of Movement Disorder. Caspian.J.Neurol.Sci. 2016; 2 (5) :50-53
URL: http://cjns.gums.ac.ir/article-1-101-en.html
1- Resident of Neurology, Student Research Committee, Department of Neurology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
2- Assistant Professor of Neurology, Department of Neurology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran ; Rezaeitalabf@mums.ac.ir
Abstract:   (1617 Views)

We report a rare genetic disorder case of neuroacanthocytosis with clinical profile (oro-lingual-facial abnormal involuntary movements, neuropathy) and typical magnetic resonance findings (cerebral atrophy, bilateral caudate nuclei atrophy with dilated anterior horns of the lateral ventricles), positive family history in his brother and acanthocytosis in peripheral blood smear.

Full-Text [PDF 311 kb]   (797 Downloads) |   |   Full-Text (HTML)  (463 Views)  
Type of Study: case report | Subject: Special
Received: 2016/07/18 | Accepted: 2016/07/18 | Published: 2016/07/18

Add your comments about this article : Your username or Email:
Write the security code in the box

© 2017 All Rights Reserved | Caspian Journal of Neurological Sciences

Designed & Developed by : Yektaweb