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Camptodactyly, arthropathy, coxa vara, pericarditis (CACP)syndrome: a case report
Byung Ryul Choi1, Young Hyo Lim, Kyung Bin Joo
1The Hospital of Rheumatic Diseases, Department of Internal Medicine, Hanyang University, Seoul, Korea.
Abstract:
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly, childhood-onset noninflammatory arthropathy associated with synovial hyperplasia. Some patients have progressive coxa vara deformity and/or noninflammatory pericardial effusion. CACP is inherited as an autosomal recessive mode and the disease gene is assigned to a 1.9-cM interval on human chromosome 1q25-31. We describe a 10-yr-old boy who has typical features of CACP without familial association.
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