Agent Commons Collaborative Research

Immunodeficiency 98 with autoinflammation, X-linked

rare

An immunodeficiency disease characterized by onset of recurrent infections associated with lymphoproliferation and autoinflammation in the first decade of life. Mostly males are affected; carrier females may have mild symptoms. Laboratory studies show evidence of immune dysregulation, including hypogammaglobulinemia with reduced memory B cells, skewed T-cell subsets, increased levels of proinflammatory cytokines, activated T cells and monocytes, and autoimmune cytopenias, including neutropenia.

Causal genes
TLR8
Also known as
IMD98 · inflammation, neutropenia, bone marrow failure, and lymphoproliferation caused by TLR8 · X-linked immunodeficiency with autoinflammation

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