Evolution of Our Understanding of XIAP Deficiency

Evolution of Our Understanding of XIAP Deficiency

X-linked inhibitor of apoptosis (XIAP) deficiency is a rare inborn error of immunity first described in 2006. XIAP deficiency is characterised by immune dysregulation and a broad spectrum of clinical manifestations, including haemophagocytic lymphohistiocytosis (HLH), inflammatory bowel disease (IBD...

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Bibliographic Details
Main Authors: Anne C. A. Mudde, Claire Booth, Rebecca A. Marsh
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Pediatrics
Subjects:
XIAP deficiency
X-linked lymphoproliferative disease
haemophagocytic lymphohistiocytosis
inflammatory bowel disease
inflammasome
haematopoietic stem cell transplantation
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.660520/full

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https://www.frontiersin.org/articles/10.3389/fped.2021.660520/full

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