147 related articles for article (PubMed ID: 15608409)
1. 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. PubMed ID: 15608409
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 9550484
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 23290693
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 16037531
[TBL] [Abstract][Full Text] [Related]
5. 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; 95(3):233-6. PubMed ID: 11102929
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 12734910
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 22386609
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 23931850
[TBL] [Abstract][Full Text] [Related]
9. Camptodactyly-arthropathy-coxa vara-pericarditis syndrome and an unusual association with mitral stenosis.
Şimşekli D; Ayabakan C; Oktay A; Arnaz A; Mahmudov V; Yalçınbaş YK
Turk J Pediatr; 2024; 66(1):134-138. PubMed ID: 38523390
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 10545950
[TBL] [Abstract][Full Text] [Related]
11. Synovial pathology in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Shayan K; Ho M; Edwards V; Laxer R; Thorner PS
Pediatr Dev Pathol; 2005; 8(1):26-33. PubMed ID: 15702367
[TBL] [Abstract][Full Text] [Related]
12. Thirteen Indians with camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Singh S; Badiger VA; Balan S; Nampoothiri S; Rao AP; Shah H; Bhavani GS; Narayanan DL; Girisha KM
Clin Dysmorphol; 2024 Mar; ():. PubMed ID: 38856641
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 22678705
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 21565623
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 17587953
[TBL] [Abstract][Full Text] [Related]
16. Familial arthropathy in Saudi Arabian children: demographic, clinical, and biochemical features.
Al-Mayouf SM
Semin Arthritis Rheum; 2007 Feb; 36(4):256-61. PubMed ID: 16996580
[TBL] [Abstract][Full Text] [Related]
17. Radiological features in congenital camptodactyly, familial arthropathy and coxa vara syndrome.
Hugosson C; Bahabri S; McDonald P; al-Dalaan A; al-Mazyed A
Pediatr Radiol; 1994; 24(7):523-6. PubMed ID: 7885792
[TBL] [Abstract][Full Text] [Related]
18. An adult with cystathionine beta-synthase deficiency, camptodactyly-arthropathy-coxa vara-pericarditis syndrome, and deafness: A case report.
Donis KC; Kalil MAB; Poswar F; Kok F; Kohem CL; Poloni S; Borsatto T; Vairo FPE; Pinheiro FC; Schwartz IVD
Genet Mol Biol; 2024; 47(1):e20220335. PubMed ID: 38593426
[TBL] [Abstract][Full Text] [Related]
19. [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. PubMed ID: 21924065
[No Abstract] [Full Text] [Related]
20. Novel PRG4 mutations underlie CACP in Saudi families.
Alazami AM; Al-Mayouf SM; Wyngaard CA; Meyer B
Hum Mutat; 2006 Feb; 27(2):213. PubMed ID: 16429407
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
