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Neuroacanthocytosis in Two Brothers: An Ultra-rare Cause of Movement Disorder

Publish place: Caspian Journal of Neurological Sciences، Vol: 2، Issue: 5
Publish Year: 1395
Type: Journal paper
Language: English
View: 373

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Link to this Paper:
https://civilica.com/doc/836068

Document National Code:

JR_CJNS-2-5_007

Index date: 9 March 2019

Neuroacanthocytosis in Two Brothers: An Ultra-rare Cause of Movement Disorder 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.

Neuroacanthocytosis in Two Brothers: An Ultra-rare Cause of Movement Disorder Keywords:

Neuroacanthocytosis , Chorea , Dystonia , Magnetic Resonance Imaging

Neuroacanthocytosis in Two Brothers: An Ultra-rare Cause of Movement Disorder authors

Ali Ghabeli-Juibary

MD, Resident of Neurology, Student Research Committee, Department of Neurology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran

Fariborz Rezaeitalab

MD, Assistant Professor of Neurology, Department of Neurology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran