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Neuroacanthocytosis in Two Brothers: An Ultra-Rare Cause of Movement Disorder
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نویسنده
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Ghabeli-Juibary Ali ,Rezaeitalab Fariborz
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منبع
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Caspian Journal Of Neurological Sciences - 2016 - دوره : 2 - شماره : 5 - صفحه:50 -53
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چکیده
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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.
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کلیدواژه
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Neuroacanthocytosis; Chorea; Dystonia; Magnetic Resonance Imaging
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آدرس
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Mashhad University Of Medical Sciences, Faculty Of Medicine, Research Committee, Department Of Neurology, ایران, Mashhad University Of Medical Sciences, School Of Medicine, Department Of Neurology, ایران
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Authors
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