275 related articles for article (PubMed ID: 27224999)
1. 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; 14(1):32. PubMed ID: 27224999
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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. PubMed ID: 29397575
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Syndrome of progressive deforming non-inflammatory arthritis of childhood: two patients of camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Johnson N; Chaudhary H; Kumrah R; Pilania RK; Sharma Y; Sharma A; Kaur A; Mukherjee S; Kakkar N; Vignesh P
Rheumatol Int; 2021 Oct; 41(10):1875-1882. PubMed ID: 32813152
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 25297354
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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(Suppl 2):S284-S287. PubMed ID: 27751317
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.
Taşar M; Eyileten Z; Kasımzade F; Uçar T; Kendirli T; Uysalel A
Turk J Pediatr; 2014; 56(6):684-6. PubMed ID: 26388606
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 23756439
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report.
Bağrul İ; Ceylaner S; Yildiz YT; Tuncez S; Aydin EA; Bağlan E; Ozdel S; Bülbül M
Pediatr Rheumatol Online J; 2023 Jan; 21(1):8. PubMed ID: 36694203
[TBL] [Abstract][Full Text] [Related]
16. Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey.
Kisla Ekinci RM; Balci S; Dogan H; Ceylaner S; Varan C; Erdem S; Coban F; Bisgin A
Mol Syndromol; 2021 Apr; 12(2):112-117. PubMed ID: 34012381
[TBL] [Abstract][Full Text] [Related]
17. Camptodactyly-arthropathy-coxa vara-pericarditis syndrome: important differential for juvenile idiopathic arthritis.
Kakkar RM; Soneji S; Badhe RR; Desai SB
J Clin Imaging Sci; 2013; 3():24. PubMed ID: 24083061
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 27748313
[No Abstract] [Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]