Camptodactyly-arthropathy-coxa vara-pericarditis syndrome

Camptodactyly-arthropathy-coxa-vara-pericarditis (CACP) syndrome is a rare, genetic, rheumatologic disease characterized by congenital or early-onset camptodactyly and symmetrical, polyarticular, non-inflammatory, large joint arthropathy with synovial hyperplasia, as well as progressive coxa vara deformity and, occasionally, non-inflammatory pericarditis.

Also known as: CACP, CACP syndrome, Jacobs syndrome, PAC syndrome, arthropathy-camptodactyly syndrome, camptodactyly-arthropathy-coxa vara-pericarditis syndrome, camptodactyly-arthropathy-pericarditis syndrome, pericarditis-arthropathy-camptodactyly syndrome

4 clinical trials for this condition and its sub-types, 4 tagged with Camptodactyly-arthropathy-coxa vara-pericarditis syndrome itself.