Title of article
Neuroacanthocytosis in Two Brothers: An Ultra-rare Cause of Movement Disorder
Author/Authors
Ghabeli-Juibary، Ali نويسنده Department of Neurology, Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Iran , , Rezaeitalab، Fariborz نويسنده Assistant professor of Neurology, Department of Neurology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran ,
Issue Information
فصلنامه با شماره پیاپی 5 سال 2016
Pages
4
From page
50
To page
53
Abstract
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.
Journal title
Caspian Journal of Neurological Sciences
Serial Year
2016
Journal title
Caspian Journal of Neurological Sciences
Record number
2391414
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