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Concurrence of myotonic dystrophy and epilepsy: a case report
INTRODUCTION: Myotonic dystrophy is a clinically and genetically heterogeneous multisystem disorder with a prevalence of 1 in 8000 in the general population. CASE PRESENTATION: A 25-year-old Ethiopian man presented with symptoms of myotonia, muscle wasting, gait problems, frontal baldness, and famil...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301074/ https://www.ncbi.nlm.nih.gov/pubmed/25496057 http://dx.doi.org/10.1186/1752-1947-8-427 |