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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Mov Disord Clin Pract
Autores principales: Rohani, Mohammad, Lang, Anthony E., Sina, Farzad, Elahi, Elahe, Fasano, Alfonso, Hardy, John, Bras, Jose, Alavi, Afagh
Formato: Artigo
Lenguaje:Inglês
Publicado: John Wiley and Sons Inc. 2017
Materias:
Case Series
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares