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Annotated abstract

CACP syndrome and PRG4 mutation

bmjcr · 2025-09-21 · canonical JSON source

1 visible annotations · policy: published · automated confidence ≥ 75.00%

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We report the case of a patient with a late diagnosis of camptodactyly–arthropathy–coxa vara–pericarditis syndrome, following his first episode of constrictive pericarditis in adulthood. We also aim to review the existing literature on this rare disease.