A toddler with an unusually severe polyarticular arthritis and a lung involvement: a case report
Abstract 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 associa...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2022-11-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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