RT Journal Article
SR Electronic
T1 Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: The First Familial Case in China and Novel Mutations of the Proteoglycan 4 Gene
JF The Journal of Rheumatology
JO J Rheumatol
FD The Journal of Rheumatology
SP jrheum.220236
DO 10.3899/jrheum.220236
A1 Jun-Mei Zhang
A1 Feng-Qiao Gao
A1 Cai-Feng Li
A1 Wei-Ying Kuang
A1 Jiang-Hong Deng
A1 Xiao-Hua Tan
A1 Chao Li
A1 Shi-Peng Li
YR 2022
UL http://www.jrheum.org/content/early/2022/09/11/jrheum.220236.abstract
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