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Items: 1 to 20 of 127

1.

Total hip arthroplasty in adolescents with severe hip arthropathy and dysplasia associated with camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

Murphy JM, Vanderhave KL, Urquhart AG.

J Arthroplasty. 2012 Sep;27(8):1581.e5-8. doi: 10.1016/j.arth.2012.01.007. Epub 2012 Mar 3.

PMID:
22386609
2.

Axial involvement with facet joint arthropathy and bony ankylosis in a case of camptodactyly, arthropathy, coxa vara, pericarditis (CACP) syndrome.

Emad Y, Ragab Y, Khalifa M, Bassyouni I, El-Shaarawy N, Rasker JJ.

Joint Bone Spine. 2013 Oct;80(5):520-2. doi: 10.1016/j.jbspin.2013.01.010. Epub 2013 Aug 6.

PMID:
23931850
3.

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

Peters B, Schuurs-Hoeijmakers JH, Fuijkschot J, Reimer A, van der Flier M, Lugtenberg D, Hoppenreijs EP.

Pediatr Rheumatol Online J. 2016 May 25;14(1):32. doi: 10.1186/s12969-016-0093-5.

4.

Camptodactyly-arthropathy-coxavara-pericarditis syndrome in Saudi Arabia: clinical and molecular genetic findings in 22 patients.

Albuhairan I, Al-Mayouf SM.

Semin Arthritis Rheum. 2013 Oct;43(2):292-6. doi: 10.1016/j.semarthrit.2012.11.004. Epub 2013 Jan 2.

PMID:
23290693
5.

The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1.

Bahabri SA, Suwairi WM, Laxer RM, Polinkovsky A, Dalaan AA, Warman ML.

Arthritis Rheum. 1998 Apr;41(4):730-5.

PMID:
9550484
6.

Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.

Taşar M, Eyileten Z, Kasımzade F, Uçar T, Kendirli T, Uysalel A.

Turk J Pediatr. 2014 Nov-Dec;56(6):684-6.

PMID:
26388606
7.

A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.

Akawi NA, Ali BR, Al-Gazali L.

Birth Defects Res A Clin Mol Teratol. 2012 Jul;94(7):553-6. doi: 10.1002/bdra.23031. Epub 2012 Jun 8.

PMID:
22678705
8.

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

Nandagopalan RS, Phadke SR, Dalal AB, Ranganath P.

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

9.

Camptodactyly, arthropathy, coxa vara, pericarditis (CACP)syndrome: a case report.

Choi BR, Lim YH, Joo KB, Paik SS, Kim NS, Lee JK, Yoo DH.

J Korean Med Sci. 2004 Dec;19(6):907-10.

10.

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

Vutukuru R, Reddy KK.

Indian J Med Res. 2016 Jun;143(6):834-835. doi: 10.4103/0971-5916.192082. No abstract available.

11.

[Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis syndrome: a case report].

Li XL, Liu YL, Fu SM.

Zhonghua Er Ke Za Zhi. 2011 Jun;49(6):471-3. Chinese. No abstract available.

PMID:
21924065
12.

Brothers with constrictive pericarditis - A novel mutation in a rare disease.

Patil DV, Phadke MS, Pahwa JS, Dalal AB.

Indian Heart J. 2016 Sep;68 Suppl 2:S284-S287. doi: 10.1016/j.ihj.2016.03.020. Epub 2016 Apr 15.

13.

Camptodactyly-arthropathy-coxa vara-pericarditis syndrome versus juvenile idiopathic arthropathy.

Offiah AC, Woo P, Prieur AM, Hasson N, Hall CM.

AJR Am J Roentgenol. 2005 Aug;185(2):522-9.

PMID:
16037531
14.

CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort.

Ciullini Mannurita S, Vignoli M, Bianchi L, Kondi A, Gerloni V, Breda L, Ten Cate R, Alessio M, Ravelli A, Falcini F, Gambineri E.

Eur J Hum Genet. 2014 Feb;22(2):197-201. doi: 10.1038/ejhg.2013.123. Epub 2013 Jun 12.

15.

A novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericarditis syndrome in a consanguineous pakistani family.

Basit S, Iqbal Z, Umicevic-Mirkov M, Kamran Ul-Hassan Naqvi S, Coenen M, Ansar M, van Bokhoven H, Ahmad W.

Arch Med Res. 2011 Feb;42(2):110-4. doi: 10.1016/j.arcmed.2011.04.006.

PMID:
21565623
16.

Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

Faivre L, Prieur AM, Le Merrer M, Hayem F, Penet C, Woo P, Hofer M, Dagoneau N, Sermet I, Munnich A, Cormier-Daire V.

Am J Med Genet. 2000 Nov 27;95(3):233-6.

PMID:
11102929
17.

Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.

Yilmaz S, Uludağ Alkaya D, Kasapçopur Ö, Barut K, Akdemir ES, Celen C, Youngblood MW, Yasuno K, Bilguvar K, Günel M, Tüysüz B.

Mol Genet Genomic Med. 2018 Mar;6(2):230-248. doi: 10.1002/mgg3.364. Epub 2018 Feb 4.

18.

Syndrome of camptodactyly, arthropathy and coxa vara (CAC syndrome).

Bahabri S, Sakati N, Hugosson C, Hainau B, Al-Balla SR, Al-Mazyed A, Al-Dalaan A.

Ann Saudi Med. 1994 Nov;14(6):479-82.

19.

Camptodactyly, arthropathy, coxa vara, and pericarditis syndrome among egyptians.

El-Garf A, Mahmoud G, Gheith R, Abd El-Aaty G, Abd El-Aaty H.

J Rheumatol. 2003 May;30(5):1081-6.

PMID:
12734910
20.

CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

Marcelino J, Carpten JD, Suwairi WM, Gutierrez OM, Schwartz S, Robbins C, Sood R, Makalowska I, Baxevanis A, Johnstone B, Laxer RM, Zemel L, Kim CA, Herd JK, Ihle J, Williams C, Johnson M, Raman V, Alonso LG, Brunoni D, Gerstein A, Papadopoulos N, Bahabri SA, Trent JM, Warman ML.

Nat Genet. 1999 Nov;23(3):319-22.

PMID:
10545950

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