Secondary C1q Deficiency in Activated PI3Kδ Syndrome Type 2

Monogenic forms of vasculitis are rare but increasingly recognized. Furthermore, genetic immunodeficiency is increasingly associated with inflammatory immune dysregulatory features, including vasculitis. This case report describes a child of non-consanguineous parents who presented with chronic digi...

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Dades bibliogràfiques
Publicat a:Front Immunol
Autors principals: Hong, Ying, Nanthapisal, Sira, Omoyinmi, Ebun, Olbrich, Peter, Neth, Olaf, Speckmann, Carsten, Lucena, Jose Manuel, Gilmour, Kimberly, Worth, Austen, Klein, Nigel, Eleftheriou, Despina, Brogan, Paul
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2019
Matèries:
Immunology
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6859795/
https://ncbi.nlm.nih.gov/pubmed/31781101
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.02589
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