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

BACKGROUND: 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 bet...

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Detalles Bibliográficos
Autores principales: Basile, Pietro, Gortani, Giulia, Taddio, Andrea, Pastore, Serena, Corona, Federica, Tesser, Alessandra, Barbi, Egidio, Tommasini, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635076/
https://www.ncbi.nlm.nih.gov/pubmed/36333696
http://dx.doi.org/10.1186/s12887-022-03716-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635076/
https://www.ncbi.nlm.nih.gov/pubmed/36333696
http://dx.doi.org/10.1186/s12887-022-03716-1

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