Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis

BACKGROUND: Severe combined immunodeficiency (SCID) syndromes are a heterogenous group of diseases characterized by impairment in both cellular and humoral immunity with a range of genetic disorders. Complete recombinase activating gene (RAG) deficiency is associated with classical T(-)B(-)NK(+) SCI...

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Detalles Bibliográficos
Autores principales: Ulusoy, Ezgi, Karaca, Neslihan Edeer, Azarsiz, Elif, Berdeli, Afig, Aksu, Guzide, Kutukculer, Necil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817577/
https://www.ncbi.nlm.nih.gov/pubmed/27081423
http://dx.doi.org/10.14740/jocmr2316w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817577/
https://www.ncbi.nlm.nih.gov/pubmed/27081423
http://dx.doi.org/10.14740/jocmr2316w

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