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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3662572/
https://ncbi.nlm.nih.gov/pubmed/23692804
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-8-79
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