PT  - JOURNAL ARTICLE
AU  - Jun-Mei Zhang
AU  - Feng-Qiao Gao
AU  - Cai-Feng Li
AU  - Wei-Ying Kuang
AU  - Jiang-Hong Deng
AU  - Xiao-Hua Tan
AU  - Chao Li
AU  - Shi-Peng Li
TI  - Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: The First Familial Case in China and Novel Mutations of the Proteoglycan 4 Gene
AID  - 10.3899/jrheum.220236
DP  - 2022 Sep 15
TA  - The Journal of Rheumatology
PG  - jrheum.220236
4099  - http://www.jrheum.org/content/early/2022/09/11/jrheum.220236.short
4100  - http://www.jrheum.org/content/early/2022/09/11/jrheum.220236.full
AB  - Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome is a rare autosomal recessive disorder characterized by camptodactyly, noninflammatory arthropathy, progressive coxa vara, and aseptic pericarditis. It is more common in countries with high rates of consanguineous marriage, such as Saudi Arabia, the United Arab Emirates, and Pakistan.1-3