Data Sheet 1_Musculoskeletal ultrasound discriminating camptodactyly-arthropathy-coxa vara

A retrospective multicentre analysis of MSUS images from 10 children compared genetically confirmed Camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) to active polyarticular juvenile idiopathic arthritis (JIA). Hatice Adigüzel Dundar authored the study, which was last updated on 2026-06-04. The 181.7 KB PDF likely contains qualitative and semi-quantitative assessments of joint and tendon findings.

Use Cases

• Develop criteria for discriminating CACP from JIA based on symmetrical joint involvement and effusion patterns.
• Train models to identify hyperechoic foci suggestive of increased synovial fluid viscosity.
• Analyze the absence of intrasynovial Doppler signal as a diagnostic marker for CACP.
• Compare tendon hypervascularity patterns between CACP and inflammatory arthritis cohorts.

Strengths

• Data originates from a retrospective multicentre analysis, suggesting multi-source validation.
• Findings are based on scans from 10 children, with specific counts provided for joint and tendon observations.
• Uses standardized OMERACT definitions for semi-quantitative grading (0–3).

Limitations

• Row count is unknown, which may limit suitability assessment.
• Column-level documentation is absent; field semantics must be inferred after download.
• The dataset is very small at 181.7 KB, indicating limited scope.

Provenance

Source

figshare

Collection Method

Retrospective multicentre analysis of MSUS images from children with genetically confirmed CACP or a diagnosis of active polyarticular JIA.

Freshness

Last updated 2026-06-04 05:42:48; freshness should be verified.