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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Detalles Bibliográficos
Autores principales: Duchatelet, Sabine, Hovnanian, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373112/
https://www.ncbi.nlm.nih.gov/pubmed/25886873
http://dx.doi.org/10.1186/s13023-015-0246-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4373112/
https://www.ncbi.nlm.nih.gov/pubmed/25886873
http://dx.doi.org/10.1186/s13023-015-0246-5

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