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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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| Gepubliceerd in: | J Med Case Rep |
|---|---|
| Hoofdauteur: | |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4301074/ https://ncbi.nlm.nih.gov/pubmed/25496057 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-8-427 |
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