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.
2022
4-nov-2022
Pubblicato
https://bmcpediatr.biomedcentral.com/articles/10.1186/s12887-022-03716-1
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635076/
File in questo prodotto:
File Dimensione Formato  
COPA.pdf

accesso aperto

Tipologia: Documento in Versione Editoriale
Licenza: Creative commons
Dimensione 2.78 MB
Formato Adobe PDF
2.78 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3033118
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 3
  • ???jsp.display-item.citation.isi??? 3
social impact