Camptodactyly-arthropathy-coxa-vara-pericarditis (CACP) syndrome is a rare, genetic, rheumatologic disease characterized by congenital or early-onset camptodactyly and symmetrical, polyarticular, non-inflammatory, large joint arthropathy with synovial hyperplasia, as well as progressive coxa vara deformity and, occasionally, non-inflammatory pericarditis.
Genes related to Camptodactyly-arthropathy-coxa-vara-pericarditis Syndrome
Clinical FeaturesTop most frequent phenotypes and symptoms related to Camptodactyly-arthropathy-coxa-vara-pericarditis Syndrome
- Flexion contracture
- Skin rash
- Abnormality of the foot
- Abdominal distention
- Chest pain
- Mitral valve prolapse
And another 28 symptoms. If you need more information about this disease we can help you.
Incidence and onset information— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.
Camptodactyly-arthropathy-coxa-vara-pericarditis Syndrome Is also known as fibrosing serositis, familial, hypertrophic synovitis, congenital familial, pac syndrome, camptodactyly-arthropathy-pericarditis syndrome, arthropathy-camptodactyly syndrome, cacp syndrome, jacobs syndrome, pericarditis-arthropathy-camptodactyly syndrome, cap syn.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Sources and references
You can check the following sources for additional information.ORPHANET OMIM MESH Rare Disease Symptoms Checker
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