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Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report

The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly, childhood-onset noninflammatory arthropathy associated with synovial hyperplasia. Some patients have pro-gressive coxa vara deformity and/or noninflammatory pericardial e...

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Autores principales: Choi, Byung-Ryul, Lim, Young-Hyo, Joo, Kyung-Bin, Paik, Seung Sam, Kim, Nam Su, Lee, Je-kyung, Yoo, Dae-Hyun
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816297/
https://www.ncbi.nlm.nih.gov/pubmed/15608409
http://dx.doi.org/10.3346/jkms.2004.19.6.907
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author Choi, Byung-Ryul
Lim, Young-Hyo
Joo, Kyung-Bin
Paik, Seung Sam
Kim, Nam Su
Lee, Je-kyung
Yoo, Dae-Hyun
author_facet Choi, Byung-Ryul
Lim, Young-Hyo
Joo, Kyung-Bin
Paik, Seung Sam
Kim, Nam Su
Lee, Je-kyung
Yoo, Dae-Hyun
author_sort Choi, Byung-Ryul
collection PubMed
description The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly, childhood-onset noninflammatory arthropathy associated with synovial hyperplasia. Some patients have pro-gressive coxa vara deformity and/or noninflammatory pericardial effusion. CACP is inherited as an autosomal recessive mode and the disease gene is assigned to a 1.9-cM interval on human chromosome 1q25-31. We describe a 10-yr-old boy who has typical features of CACP without familial association.
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spelling pubmed-28162972010-02-04 Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report Choi, Byung-Ryul Lim, Young-Hyo Joo, Kyung-Bin Paik, Seung Sam Kim, Nam Su Lee, Je-kyung Yoo, Dae-Hyun J Korean Med Sci Case Report The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly, childhood-onset noninflammatory arthropathy associated with synovial hyperplasia. Some patients have pro-gressive coxa vara deformity and/or noninflammatory pericardial effusion. CACP is inherited as an autosomal recessive mode and the disease gene is assigned to a 1.9-cM interval on human chromosome 1q25-31. We describe a 10-yr-old boy who has typical features of CACP without familial association. The Korean Academy of Medical Sciences 2004-12 2004-12-31 /pmc/articles/PMC2816297/ /pubmed/15608409 http://dx.doi.org/10.3346/jkms.2004.19.6.907 Text en Copyright © 2004 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Choi, Byung-Ryul
Lim, Young-Hyo
Joo, Kyung-Bin
Paik, Seung Sam
Kim, Nam Su
Lee, Je-kyung
Yoo, Dae-Hyun
Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report
title Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report
title_full Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report
title_fullStr Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report
title_full_unstemmed Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report
title_short Camptodactyly, Arthropathy, Coxa vara, Pericarditis (CACP)Syndrome: A Case Report
title_sort camptodactyly, arthropathy, coxa vara, pericarditis (cacp)syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816297/
https://www.ncbi.nlm.nih.gov/pubmed/15608409
http://dx.doi.org/10.3346/jkms.2004.19.6.907
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