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Lymphoproliferative syndrome 1
rareA condition of decreased or absent presence or activity of IL2-inducible t-cell kinase. Deficiency of this protein is associated with lymphoproliferative syndrome 1, an autosomal recessive primary immunodeficiency characterized by onset in early childhood of Epstein-Barr virus (EBV)-associated immune dysregulation, manifest as lymphoma, lymphomatoid granulomatosis, hemophagocytic lymphohistiocytosis, Hodgkin disease, and/or hypogammaglobulinemia..
- Identifiers
- MONDO:0013081 OMIM:613011Orphanet:538963
- Causal genes
- ITK
- Also known as
- ITK deficiency · ITK lymphoproliferative syndrome · LPFS1 · lymphoproliferative syndrome caused by mutation in ITK · lymphoproliferative syndrome type 1
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