Literature DB >> 3964320

A familial syndrome of pericarditis, arthritis, camptodactyly, and coxa vara.

G Bulutlar, H Yazici, H Ozdoğan, I Schreuder.   

Abstract

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Year:  1986        PMID： 3964320     DOI： 10.1002/art.1780290321

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN： 0004-3591


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  5 in total

1.  Radiological features in congenital camptodactyly, familial arthropathy and coxa vara syndrome.

Authors:  C Hugosson; S Bahabri; P McDonald; A al-Dalaan; A al-Mazyed
Journal:  Pediatr Radiol       Date:  1994

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

Authors:  Byung Ryul Choi; Young Hyo Lim; Kyung Bin Joo; Seung Sam Paik; Nam Su Kim; Je Kyung Lee; Dae Hyun Yoo
Journal:  J Korean Med Sci       Date:  2004-12       Impact factor: 2.153

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

Authors:  Sara Ciullini Mannurita; Marina Vignoli; Lucia Bianchi; Anuela Kondi; Valeria Gerloni; Luciana Breda; Rebecca Ten Cate; Maria Alessio; Angelo Ravelli; Fernanda Falcini; Eleonora Gambineri
Journal:  Eur J Hum Genet       Date:  2013-06-12       Impact factor: 4.246

4.  The Efficacy of Yttrium-90 Radiosynovectomy in Patients with Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome.

Authors:  Sulaiman Mohammed Al-Mayouf; Nora Almutairi; Khalid Alismail
Journal:  Mol Imaging Radionucl Ther       Date:  2017-02-05

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

Authors:  Saliha Yilmaz; Dilek Uludağ Alkaya; Özgür Kasapçopur; Kenan Barut; Ekin S Akdemir; Cemre Celen; Mark W Youngblood; Katsuhito Yasuno; Kaya Bilguvar; Murat Günel; Beyhan Tüysüz
Journal:  Mol Genet Genomic Med       Date:  2018-02-04       Impact factor: 2.183
  5 in total

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