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 ,
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.
