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Is familial Mediterranean fever a possible cofactor for Budd-Chiari syndrome? J Pediatr Gastr Nutr 2009;49:481–4. 9 Aksu G, Ozturk C, Kavakli K, Genel F, Kutukculer N. Hypercoagulability: interaction between inflammation and coagulation in familial Mediterranean fever. Clin Rheumatol 2007;26:366–70. 10 Demirel A, Celkan T, Kasapcopur O et al. Is familial Mediterranean fever a thrombotic disease...

BACKGROUND/AIM The aim of this study was to investigate the relationship between familial Mediterranean fever and female sexual dysfunction and premenstrual syndrome. MATERIALS AND METHODS This study included 36 patients with familial Mediterranean fever and 33 healthy volunteers. Familial Mediterranean fever was diagnosed according to the Tel Hashomer criteria and familial Mediterranean feve...

Familial Mediterranean Fever, the most common autoinflammatory disease, is inherited in an autosomal recessive pattern. During the recent years, a new phenotype has been described concerning heterozygous carriers of Mediterranean Fever (MEFV) mutations that express typical clinical features of Familial Mediterranean Fever (FMF). This new pattern of genotype-phenotype correlation is called “FMF-...

BACKGROUND Familial Mediterranean Fever and celiac disease are both related to auto-inflammation and/or auto-immunity and they share some common clinical features such as abdominal pain, diarrhea, bloating and flatulence. Objectives We aimed to determine the association of these two diseases, if present. METHODS Totally 112 patients diagnosed with Familial Mediterranean Fever and 32 cases as ...

Familial Mediterranean fever is a multisystem disorder, usually seen in subjects of Mediterranean and Middle Eastern origin, characterized by recurrent bouts of fever and pain due to inflammation of the peritoneum, synovia, or pleura. In this article we report a case of Familial Mediterranean fever with recurrent abdominal pain and hyperbilirubinemia, review the literature and discuss whether t...

Background. Eosinophilic esophagitis is an inflammatory condition where there is a dense infiltration of eosinophils typically exceeding fifteen cells per high power field. Familial Mediterranean fever is an autosomal recessive disorder characterized by brief, acute, and self-limited episodes of fever and polyserositis that recur at irregular intervals. Case Presentation. A three-year-and-nine-...

background: blood neutrophil to lymphocyte ratio (nlr) and mean platelet volume (mpv) both have been used as a simple marker of inflammation in many disorders. here, we aimed to investigate the relationship between nlr, mpv, and familial mediterranean fever (fmf). materials and methods: in this retrospective study, the fi les of fmf patients in pediatric rheumatology outpatient clinic were revi...