ArticleEuropean journal of rheumatology2016
The role of MEFV mutations in the concurrent disorders observed in patients with familial Mediterranean fever.
Article in European journal of rheumatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
7 citing papers in PubMed, 16 citations in OpenAlex.
- Familial Mediterranean Fever Mutation Analysis in Pediatric Patients With İnflammatory Bowel Disease: A Multicenter Study.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2021Article
- Evaluation of co-existing diseases in children with familial Mediterranean fever.Rheumatology international · 2020Article
- The musculoskeletal system manifestations in children with familial Mediterranean fever.Northern clinics of Istanbul · 2020Article
- Familial mediterranean fever: assessment of clinical manifestations, pregnancy, genetic mutational analyses, and disease severity in a national cohort.Rheumatology international · 2020Article
- Frequency of functional gastrointestinal disorders in children with familial Mediterranean fever.Clinical rheumatology · 2019Article
- Familial Mediterranean Fever in Chinese Children: A Case Series.Frontiers in pediatrics · 2019Article
- The Influence of Concomitant Disorders on Disease Severity of Familial Mediterranean Fever in Children.Archives of rheumatology · 2018Article
Corrections and comments
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Authors and funding
5 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveThis study aimed to investigate the frequency in which familial Mediterranean fever (FMF) coexists with other diseases and determine whether Mediterranean fever MATERIAL AND
methodsIn total, 142 consecutive patients with FMF investigated for
resultsConcomitant disorders were found in 17 of 73 patients with FMF (23%) in Group I and 5 of 56 patients (8.9%) in Group II (p=0.04). Concomitant disorders in Group I were as follows: 7 cases of amyloidosis, 2 cases of Behcet's disease (BD), 4 cases of ankylosing spondylitis (AS), 1 case of antiphospholipid syndrome, 1 case of Henoch-Schonlein purpura (HSP), 1 case of combination of psoriatic arthritis, HSP, and membranoproliferative glomerulonephritis, and 1 case of AS and amyloidosis. In Group II, the following disorders were found: 1 case of amyloidosis, 1 case of BD, 1 case of AS, 1 case of ulcerative colitis, and 1 case of vitiligo.
conclusionThe presence of M694V mutation may predispose patients with FMF to developing other inflammatory disorders.
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