51. Neuroacanthocytosis in Two Brothers: An Ultra-rare Cause of Movement Disorder
- Author
-
Fariborz Rezaeitalab and Ali Ghabeli-Juibary
- Subjects
medicine.medical_specialty ,business.industry ,Movement (music) ,Neuroscience (miscellaneous) ,medicine.disease ,Magnetic Resonance Imaging ,lcsh:RC346-429 ,lcsh:RC321-571 ,Psychiatry and Mental health ,Dystonia ,Physical medicine and rehabilitation ,Neurology ,Chorea ,Neuroacanthocytosis ,medicine ,Neurology (clinical) ,business ,lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry ,lcsh:Neurology. Diseases of the nervous system - 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.
- Published
- 2016