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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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| Udgivet i: | Orphanet J Rare Dis |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2015
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| Fag: | |
| Online adgang: | 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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