/camptodactyly-arthropathy-coxa vara-pericarditis syndrome

camptodactyly-arthropathy-coxa vara-pericarditis syndrome

Rare Disease

MONDO:0008828

Also Known As

CACPCACP syndromeJacobs syndromePAC syndromearthropathy-camptodactyly syndromecamptodactyly-arthropathy-coxa vara-pericarditis syndromecamptodactyly-arthropathy-pericarditis syndromecongenital familial hypertrophic synovitisfamilial fibrosing serositispericarditis-arthropathy-camptodactyly syndromearthropathy camptodactyly syndromecamptodactyly arthropathy coxa vara pericarditis syndromecamptodactyly arthropathy pericarditis syndromecamptodactyly-arthropathy-coxa-vara-pericarditis syndromefibrosing serositis, familialhypertrophic synovitis, congenital familialpericarditis arthropathy camptodactyly syndrome

Definition

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.