Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).

X-linked lymphoproliferative syndromes (XLP) are primary immunodeficiencies characterized by a particular vulnerability toward Epstein-Barr virus infection, frequently resulting in hemophagocytic lymphohistiocytosis (HLH). XLP type 1 (XLP-1) is caused by mutations in the gene SH2D1A (also named SAP)...

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Detalles Bibliográficos
Autores principales: Pachlopnik Schmid, J, Canioni, D, Moshous, D, Touzot, F, Mahlaoui, N, Hauck, F, Kanegane, H, Lopez-Granados, E, Mejstrikova, E, Pellier, I, Galicier, L, Galambrun, C, Barlogis, V, Bordigoni, P, Fourmaintraux, A, Hamidou, M, Dabadie, A, Le Deist, F, Haerynck, F, Ouachée-Chardin, M, Rohrlich, P, Stephan, J, Lenoir, C, Rigaud, S, Lambert, N
Formato: Journal article
Lenguaje:English
Publicado: 2011

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