Literature DB >> 18314374

Neuroacanthocytosis and carbamazepine responsive paroxysmal dyskinesias.

Lorena Tschopp1, Gabriela Raina, Zulema Salazar, Federico Micheli.   

Abstract

Neuroacanthocytosis (NA) comprises a genetically heterogeneous group of disorders characterized by dysfunction of the erythrocyte membrane, presenting with acanthocytes and several neurological manifestations. We report the case of a 42-year-old woman with NA who in addition had episodes consistent with paroxysmal dyskinesias. She was diagnosed with NA featuring mild chorea, weakness of the right lower extremity and myoclonic jerks. However, one year after onset she presented attacks of paroxysmal abnormal movements, consistent with paroxysmal kinesigenic dyskinesias. Carbamazepine markedly reduced the frequency and severity of the attacks. Our case illustrates that paroxysmal dyskinesias can be a hitherto unrecognized manifestation of neuroacanthocytosis responsive to carbamazepine.

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Year:  2008        PMID: 18314374     DOI: 10.1016/j.parkreldis.2007.10.006

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  3 in total

1.  Paroxysmal dyskinesias.

Authors:  Shyamal H Mehta; John C Morgan; Kapil D Sethi
Journal:  Curr Treat Options Neurol       Date:  2009-05       Impact factor: 3.598

2.  Use of antiepileptic drugs for hyperkinetic movement disorders.

Authors:  A Siniscalchi; L Gallelli; G De Sarro
Journal:  Curr Neuropharmacol       Date:  2010-12       Impact factor: 7.363

Review 3.  Neuroacanthocytosis syndromes.

Authors:  Hans H Jung; Adrian Danek; Ruth H Walker
Journal:  Orphanet J Rare Dis       Date:  2011-10-25       Impact factor: 4.123

  3 in total

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