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Monogenic type I interferonopathies are inherited heterogeneous disorders featured by early-onset of systemic and organ specific inflammation, associated with constitutive activation of type I interferons (IFNs). The knowledge of clinical profiles with which they manifest and of the pathogenetic mechanisms is fundamental for clinicians mainly dedicated to rare diseases and also for researchers in order to understand other parenchymal lung disorders
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This page is a summary of: Lung involvement in monogenic interferonopathies, European Respiratory Review, December 2020, European Respiratory Society (ERS),
DOI: 10.1183/16000617.0001-2020.
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