A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey2021 · 23 citations
2. 2Camptodactyly-arthropathy-coxavara-pericarditis syndrome in Saudi Arabia: Clinical and molecular genetic findings in 22 patients2013 · 35 citations
3. 3Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (<scp>CACP</scp>) syndrome2018 · 37 citations
4. 4Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.2014 · 11 citations
5. 5A novel mutation in <i>PRG4</i> gene underlying camptodactyly‐arthropathy‐coxa vara‐pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract2012 · 21 citations