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Cutaneous Manifestations of DOCK8 Deficiency Syndrome
BACKGROUND: Mutations in the dedicator of cytokinesis 8 gene (DOCK8) cause a combined primary immunodeficiency syndrome that is characterized by elevated serum IgE levels, depressed IgM levels, eosinophilia, sinopulmonary infections, cutaneous viral infections, and lymphopenia. Many patients with DO...
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| Principais autores: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4103903/ https://ncbi.nlm.nih.gov/pubmed/21931011 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archdermatol.2011.262 |
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