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A Case of Lafora Disease Diagnosed by Axillary Skin Biopsy
Lafora disease is a severe form of progressive myoclonic epilepsy with autosomal recessive inheritance diagnosed by inclusion body in biopsy. A 26-year-old woman was admitted due to complaints of frequent twitches and fainting. The 0.5x0.3x0.3 cm axillary skin punch biopsy was subjected to routine h...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Federation of Turkish Pathology Societies
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510617/ https://www.ncbi.nlm.nih.gov/pubmed/33432562 http://dx.doi.org/10.5146/tjpath.2021.01522 |