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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Mov Disord Clin Pract
Egile Nagusiak: Rohani, Mohammad, Lang, Anthony E., Sina, Farzad, Elahi, Elahe, Fasano, Alfonso, Hardy, John, Bras, Jose, Alavi, Afagh
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: John Wiley and Sons Inc. 2017
Gaiak:
Case Series
Sarrera elektronikoa: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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