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: Pietro Basile (Author), Giulia Gortani (Author), Andrea Taddio (Author), Serena Pastore (Author), Federica Corona (Author), Alessandra Tesser (Author), Egidio Barbi (Author), Alberto Tommasini (Author)
Format: Book
Published: BMC, 2022-11-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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