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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Chu, Emily Y., Freeman, Alexandra F., Jing, Huie, Cowen, Edward W., Davis, Joie, Su, Helen C., Holland, Steven M., Chanco Turner, Maria L.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 2011
विषय:
ऑनलाइन पहुंच: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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