COPA syndrome is a rare hereditary inflammatory disease caused by mutations in the gene encoding the coatomer protein subunit alpha, causing excessive production of type I interferon. This case is a reminder for the general paediatrician, highlighting the relevance of the association between arthritis and lung involvement in toddlers.

A toddler with an unusually severe polyarticular arthritis and a lung involvement: a case report

Gortani, Giulia;Taddio, Andrea;Pastore, Serena;Corona, Federica;Tesser, Alessandra;Barbi, Egidio;Tommasini, Alberto
2022

Abstract

COPA syndrome is a rare hereditary inflammatory disease caused by mutations in the gene encoding the coatomer protein subunit alpha, causing excessive production of type I interferon. This case is a reminder for the general paediatrician, highlighting the relevance of the association between arthritis and lung involvement in toddlers.
4-nov-2022
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https://bmcpediatr.biomedcentral.com/articles/10.1186/s12887-022-03716-1
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635076/
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3033118
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