Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome

Common Name(s)

Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome

The camptodactyly-arthropathy-coxa vara-pericarditis syndrome is an autosomal recessive condition characterized by the association of congenital or early-onset camptodactyly and noninflammatory arthropathy with synovial hyperplasia. Progressive coxa vara deformity and/or noninflammatory pericardial or pleural effusions are found in some patients (summary by {4:Faivre et al., 2000}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome" returned 4 free, full-text research articles on human participants. First 3 results:

Pathognomonic acetabular cysts in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.
 

Author(s): Ravindranath Vutukuru, Kotha Krishna Mohan Reddy

Journal: Indian J. Med. Res.. 2016 Jun;143(6):834-835.

 

Last Updated: 17 Oct 2016

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Protein-losing enteropathy in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.
 

Author(s): Bram Peters, Janneke H M Schuurs-Hoeijmakers, Joris Fuijkschot, Annette Reimer, Michiel van der Flier, Dorien Lugtenberg, Esther P A H Hoppenreijs

Journal:

 

Camptodactyly-arthropathy-coxa vara-pericarditis (CACP, OMIM: #208250) syndrome is a rare autosomal recessive disease that can be difficult to recognise not only because of its wide clinical variability but also because of its clinical resemblance to juvenile idiopathic arthritis ...

Last Updated: 26 May 2016

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Novel mutations in PRG4 gene in two Indian families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.
 

Author(s): Rajashree S Nandagopalan, Shubha R Phadke, Ashwin B Dalal, Prajnya Ranganath

Journal: Indian J. Med. Res.. 2014 Aug;140(2):221-6.

 

Camptodactyly--arthropathy-coxa vara-pericarditis (CACP) syndrome is an autosomal recessive disorder caused by mutations in the PRG4 (proteoglycan 4) gene. Hallmarks of the syndrome include congenital or early-onset camptodactyly and arthropathy with synovial hyperplasia, progressive ...

Last Updated: 9 Oct 2014

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome" returned 0 free, full-text review articles on human participants.

 
 
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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Brain Imaging of Childhood Onset Psychiatric Disorders, Endocrine Disorders and Healthy Volunteers
 

Status: Recruiting

Condition Summary: XXY (Klinefelter); Sex Chromosome Variation; Sex Chromosome Aneuploidy; XXXY; XXXXXY; XYY (Jacob); XXYY; X (XO, Turner); XXX (Trisomy X, Triple X); XXXX (Tetrasomy X); XXXXX (Pentasomy X)

 

Last Updated: 7 Nov 2017

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