eating dystonia in a case of neuroacanthocytosis.

نویسندگان

mohammad rohani department of neurology, school of medicine, rasoul akram hospital, iran university of medical sciences, tehran, iran.

gholamali shahidi department of neurology, school of medicine, rasoul akram hospital, iran university of medical sciences, tehran, iran.

چکیده

no abstract

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Eating dystonia in a case of neuroacanthocytosis

Neuroacanthocytosis is an autosomal recessive neurodegenerative disease, characterized by chorea, dementia, seizure, acanthocytes on peripheral blood smear and caudate atrophy on brain magnetic resonance imaging (MRI).1,2 These patients have severe orofacial dyskinesia and especially eating dystonia that causes severe eating problems and tongue and cheek biting. Eating or feeding dystonia, in c...

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Feeding dystonia: A classical presentation of neuroacanthocytosis

Introduction: Neuroacanthocytosis (NA) is a heterogeneous neurodegenerative genetic disorder caused by disease specific genetic mutation. Being an extremely rare disorder, only a few thousand cases have been reported till date. This clinical entity was described by Citchley et al. and was initially named Levine–Citchley syndrome. It is characterized by movement disorder due to degeneration of t...

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Neuroacanthocytosis : a Case Report

An adult male with severe tic disorder presented with recurrent injury to tongue and dysphagia. There were a significant excess of acanthocytes in the peripheral blood smear. Treatment with lithium resulted in a considerable reduction in the severity of tics and self-injurious behaviour.

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Choreoacanthocytosis, more broadly called neuroacanthocytosis, is a rare neurodegenerative disorder usually inherited as an autosomal recessive trait. It is one of the neuroacanthocytosis syndromes characterized by neurological problems and acanthocytosis. Symptoms typically become apparent between the ages of 25 and 45. The disorder may be characterized by chorea, dystonia, a buckling gait, ti...

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عنوان ژورنال:
iranian journal of neurology

جلد ۱۴، شماره ۱، صفحات ۵۲-۰

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