Olmsted syndrome: exploration of the immunological phenotype

BACKGROUND: Olmsted syndrome is a rare congenital skin disorder presenting with periorifical hyperkeratotic lesions and mutilating palmoplantar keratoderma, which is often associated with infections of the keratotic area. A recent study identified de novo mutations causing constitutive activation of...

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Detalles Bibliográficos
Autores principales: Danso-Abeam, Dina, Zhang, Jianguo, Dooley, James, Staats, Kim A, Van Eyck, Lien, Van Brussel, Thomas, Zaman, Shari, Hauben, Esther, Van de Velde, Marc, Morren, Marie-Anne, Renard, Marleen, Van Geet, Christel, Schaballie, Heidi, Lambrechts, Diether, Tao, Jinsheng, Franckaert, Dean, Humblet-Baron, Stephanie, Meyts, Isabelle, Liston, Adrian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662572/
https://www.ncbi.nlm.nih.gov/pubmed/23692804
http://dx.doi.org/10.1186/1750-1172-8-79

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662572/
https://www.ncbi.nlm.nih.gov/pubmed/23692804
http://dx.doi.org/10.1186/1750-1172-8-79

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