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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...
में बचाया:
| में प्रकाशित: | Mov Disord Clin Pract |
|---|---|
| मुख्य लेखकों: | , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
John Wiley and Sons Inc.
2017
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| विषय: | |
| ऑनलाइन पहुंच: | 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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