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Mosaic epidermolytic ichthyosis - Case report
Epidermolytic ichthyosis is a rare autosomal dominant disease that manifests at birth with fragile blisters and erosions that evolve into hyperkeratotic lesions associated or not with erythroderma. When the disease is associated with a mutation in cytokeratin 1, it may be related to hyperkeratosis o...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Sociedade Brasileira de Dermatologia
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3876022/ https://ncbi.nlm.nih.gov/pubmed/24346896 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20132203 |
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