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Epidermolysis bullosa simplex with muscular dystrophy. Review of the literature and a case report
BACKGROUND: Epidermolysis bullosa simplex associated with muscular dystrophy is a genetic skin disease caused by plectin deficiency. A case of a 19-year-old Czech patient affected with this disease and a review all previously published clinical cases are presented. MAIN OBSERVATIONS: In our patient,...
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| Publicat a: | J Dermatol Case Rep |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Specjalisci Dermatolodzy
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5385263/ https://ncbi.nlm.nih.gov/pubmed/28400893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3315/jdcr.2016.1231 |
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