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
2022-01-01
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.File in questo prodotto:
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