Literature DB >> 23832993

Familial Mediterranean fever without fever as a cause of monoarthritis.

Georg Mattiassich1, Georg Semlitsch, Karin Nadler, Franz Rainer.   

Abstract

Familial Mediterranean fever (FMF) is an autosomal recessive hereditary disease. FMF-related arthritis affects large joints, especially in the lower extremities. It starts with acute pain and swelling and affects one joint at a time. Fever is the most common symptom in FMF. Monoarthritis as the sole symptom is relatively rare and thus delayed diagnosis of the disease in a patient who had been suffering from monoarthritis for several years. Genetic analysis showing typical mutations in the patient eventually resulted in correct diagnosis, although classical clinical diagnostic criteria were not met. The patient received appropriate therapy with colchicine, which led to remission of the symptoms.

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Year:  2013        PMID: 23832993      PMCID: PMC3736377          DOI: 10.1136/bcr-2012-008395

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  11 in total

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Journal:  Z Rheumatol       Date:  2011-08       Impact factor: 1.372

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  2 in total

1.  Atypical Familial Mediterranean Fever Presenting with Recurrent Migratory Polyarthritis.

Authors:  Kentaro Iwata; Tomoko Toma; Akihiro Yachie
Journal:  Intern Med       Date:  2019-07-10       Impact factor: 1.271

2.  Familial Mediterranean fever phenotype progression into anti-cyclic citrullinated peptide antibody-positive rheumatoid arthritis:a case report.

Authors:  Toru Yago; Tomoyuki Asano; Yuya Fujita; Kiyoshi Migita
Journal:  Fukushima J Med Sci       Date:  2020-11-06
  2 in total

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