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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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| Publicat a: | Mov Disord Clin Pract |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2017
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| Matèries: | |
| Accés en línia: | 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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