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Resistin and visfatin: are they valuable enough to be the differential diagnosis in familial Mediterranean fever with acute appendicitis?

Can mean platelet volume, Neutrophil-to-Lymphocyte, Lymphocyte-to-Monocyte, Platelet-to-Lymphocyte ratios be favourable predictors for the differential diagnosis of appendicitis?

Familial Mediterranean fever is the result of mutations in the MEFV gene encoding pyrin that is a regulatory component of the intracellular inflammasome complex required for the conversion of pro-interleukin (IL)-1[beta] into active IL-1[beta].

Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicine

Familial Mediterranean fever is an autosomal recessive disease characterized by recurrent episodes of fever, peritonitis, pleuritis, and arthritis.[2] Previous studies have reported that 90% of patients have abdominal, 75% have articular, and 45% have pleural episodes.

Familial Mediterranean fever with recurrent erysipelas-like erythema and myalgia: A case report

Familial Mediterranean fever: prevalence, penetrance and genetic drift.

Can Allergen Specific Immunotherapy Induce Familial Mediterranean Fever Attacks?/Allerjen Spesifik immunoterapi Ailevi Akdeniz Atesi Ataklarini Tetikleyebilir mi?

Nailfold capillary abnormalities in patients with familial Mediterranean fever. Clin Exp Rheumatol 2001; 19: 42-4.

Nail Fold Capillary Abnormality and Insulin Resistance in Children with Familial Mediterranean Fever: Is There Any Relationship Between Vascular Changes and Insulin Resistance?

Distribution of the maternal origins of patients with familial Mediterranean fever and juvenile idiopathic arthritis by geographic regions Note: Table made from Bar-graph Distribution of the paternal origins as percentiles by geographical regions FMF JIA Black Sea 47,3 40,7 Central Anatolia 21,7 11,3 Eastern Anatolia 21,1 21,1 Marmara 3,9 12,8 Southeast 3,6 11,8 Mediterranean 1,7 0,5 Aegeon 0,7 1,6 Figure 2.

Comparison of familial Mediterranean fever and juvenile idiopathic arthritis patients according to family origin

Although very atypical in presentation, the diagnosis of familial Mediterranean fever was considered given the robust response to steroids and his Armenian descent.

A Case of Familial Mediterranean Fever with Extensive Lymphadenopathy and Complex Heterozygous Genotype Presenting in the Fourth Decade

Giovinale et al., "Familial Mediterranean fever: a review for clinical management," Joint Bone Spine, vol.

Familial Mediterranean Gene (MEFV) Mutation in Parents of Children with Familial Mediterranean Fever: What Are the Exceptions?

Clinical disease among patients heterozygous for familial Mediterranean fever. Arthritis Rheum 2009;60(6):1862-6.

AILESEL AKDENIZ ATESI (AAA) HASTALARINDA MANNOZ BAGLAYICI LEKTIN (MBL) GEN POLIMORFIZMLERI VE KLINIK OZELLIKLERLE ILISKISI/MANNOSE BINDING LECTIN (MBL) GENE POLYMORPHISMS AND THEIR RELATIONS WITH CLINICAL FEATURES IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER (FMF)

The onset age of disease, disease duration, clinical findings (fever, abdominal pain, chest pain, joint pain, and rash), dose and duration of medication, and Mediterranean fever mutation were recorded for each patient.

Deteriorated Systolic Blood Pressure Recovery and Heart Rate Recovery After Graded Exercise in Children With Familial Mediterranean Fever

Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease characterized by repeated attacks of fever abdominal pain, pleuritic chest pain, and arthritis.

Changes in cerebral blood flow in patients with familial mediterranean Fever

Alghamdi, "Familial Mediterranean fever, review of the literature," Clinical Rheumatology, vol.

Small Intestinal Bacterial Overgrowth Affects the Responsiveness to Colchicine in Familial Mediterranean Fever