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Up to: Hereditary disorder of connective tissue · Vasculitis · Type 1 interferonopathy of childhood
Deficiency of adenosine deaminase 2
A rare autoinflammatory disease characterized by a broad clinical phenotype of systemic inflammation, vasculitis, early-onset stroke, immunodeficiency and bone marrow failure. The disease typically presents in young children, although adult cases are being discovered.
This condition has no sub-types.