Action Myoclonus and Seizure in Kufor‐Rakeb Syndrome

BACKGROUND: Kufor‐Rakeb syndrome (KRS) is a rare autosomal recessive neurologic disease with diverse phenotypic features. Herein we report an Iranian KRS family with seizure and action myoclonus in addition to other typical manifestations of this syndrome. METHOD: All family members underwent carefu...

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Detalles Bibliográficos
Publicado en:Mov Disord Clin Pract
Main Authors: Rohani, Mohammad, Lang, Anthony E., Sina, Farzad, Elahi, Elahe, Fasano, Alfonso, Hardy, John, Bras, Jose, Alavi, Afagh
Formato: Artigo
Idioma:Inglês
Publicado: John Wiley and Sons Inc. 2017
Assuntos:
Case Series
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6407049/
https://ncbi.nlm.nih.gov/pubmed/30868101
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12570
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