Epstein–Barr virus infection in primary immunodeficiency
Abstract
Lymphoproliferative conditions and susceptibility to EBV
XLP-1: mutations in SH2D1A
XLP-2: mutations in XIAP
CD27 deficiency
CTPS1 deficiency
RASGRP1 deficiency
CD70 deficiency
CARMIL2 (RLTPR) deficiency
ITK deficiency
MAGT1 deficiency
Primary immunodeficiencies associated with EBV disease
Coronin 1A
STK4 deficiency
APDS
PRKCD deficiency
LPS-Responsive Beige-Like Anchor (LRBA) deficiency
ALPS
Familial HLH
ZAP70
TYK2
Non-homologous DNA end-joining deficiencies (radiosensitive SCID)
NF-κB1 and NF-κB2
CARD11 gain-of-function mutations
NK cell abnormalities and EBV
Syndromes with CID and severe EBV infection
Wiskott–Aldrich syndrome (WAS)
Ataxia telangiectasia (AT)
WHIM
Chediak–Higashi syndrome
22q11.2 deletion syndrome (Di George)
Conclusion
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