Article

CACP Syndrome: A Rare Non-inflammatory Arthropathy Often Misdiagnosed as Juvenile Idiopathic Arthritis – Clinical Insights and Diagnostic Approach

2025-08-04

Abstract excerpt

<title>Abstract</title> <p>CACP (Camptodactyly-arthropathy-coxa-vera- pericarditis) is rare autosomal recessive genetic condition characterized by progressive joint involvement at an early age. The prevalence of this condition remains unknown. It occurs due to defect in the gene PRG-4 (Proteoglycan-4) on chromosome 1q encoding for protein lubricin. Camptodactyly is non-traumatic flexion deformity of proximal inte...

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Literature Corpus work: efb6f184-d1d6-5038-b648-4c4c5ad4fc5b
DOI: 10.21203/rs.3.rs-7137225/v1

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