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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...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2022
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| Materias: | |
| 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 |