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Olmsted syndrome: clinical, molecular and therapeutic aspects
Olmsted syndrome (OS) is a rare genodermatosis classically characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma (PPK) and periorificial keratotic plaques, but which shows considerable clinical heterogeneity. The disease starts usually at birth or in early c...
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| Publicado en: | Orphanet J Rare Dis |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2015
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4373112/ https://ncbi.nlm.nih.gov/pubmed/25886873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-015-0246-5 |
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