A narrative review on the role of cytokines in the pathogenesis and treatment of familial Mediterranean fever: an emphasis on pediatric cases
A Chaaban, H Yassine, R Hammoud, R Kanaan… - Frontiers in …, 2024 - frontiersin.org
Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disease characterized
by an early onset of recurrent fever and serositis episodes. FMF is caused by mutations in …
by an early onset of recurrent fever and serositis episodes. FMF is caused by mutations in …
Efficacy and safety of anti-interleukin-1 treatment in familial Mediterranean fever patients: a systematic review and meta-analysis
Objectives FMF is the most common hereditary monogenic fever syndrome marked by
recurrent attacks of fever and polyserositis. Colchicine is the current recommended first-line …
recurrent attacks of fever and polyserositis. Colchicine is the current recommended first-line …
Feasibility of canakinumab withdrawal in colchicine-resistant familial Mediterranean fever
S Sener, V Cam, ED Batu, M Kasap Cuceoglu… - …, 2023 - academic.oup.com
Objectives There is no consensus on canakinumab treatment tapering and discontinuation
strategies in colchicine-resistant FMF patients. In this study, we aimed to establish a …
strategies in colchicine-resistant FMF patients. In this study, we aimed to establish a …
Effect of interleukin-1 antagonist on growth of children with colchicine resistant or intolerant FMF
S Pinchevski-Kadir, M Gerstein, O Pleniceanu… - Pediatric …, 2023 - Springer
Abstract Introduction Familial Mediterranean Fever (FMF) is the most common monogentic
autoinflammatory disease. FMF results from mutations in MEFV, which lead to a pro …
autoinflammatory disease. FMF results from mutations in MEFV, which lead to a pro …
[HTML][HTML] Increasing Importance of Genotype–Phenotype Correlations Associated with Common and Rare MEFV Gene Mutations in FMF Patients in the Last Thirty …
S Yildirim, H Bekis Bozkurt, M Erguven - Journal of Clinical Medicine, 2025 - mdpi.com
Background/Objectives: Studies have shown that some mutations, especially M694V, are
correlated with renal RI and/or AA. There are limited data about rare mutations on severity of …
correlated with renal RI and/or AA. There are limited data about rare mutations on severity of …
The effect of canakinumab treatment on growth parameters in children with familial Mediterranean fever
EA Aydin, E Baglan, NG Kocamaz, İ Bagrul… - Clinical …, 2024 - Springer
Introduction/objectives This study aimed to evaluate the effect of canakinumab on growth
parameters in children with familial Mediterranean fever (FMF). Method We conducted a …
parameters in children with familial Mediterranean fever (FMF). Method We conducted a …
[PDF][PDF] GENETIC, CLINICAL AND TREATMENT HETEROGENEITY IN FAMILIAL MEDITERRANEAN FEVER
J Ardui - 2023 - libstore.ugent.be
Abstract Introduction: Autoinflammatory diseases (AIDs) are caused by genetic disturbances
resulting in exaggerated innate immune responses characterized by recurrent fever attacks …
resulting in exaggerated innate immune responses characterized by recurrent fever attacks …
Heterozygous E148Q Mutation in an Indian Family with a Milder Form of Familial Mediterranean Fever
MC Abdulla - Indian Journal of Rheumatology, 2023 - journals.lww.com
Familial Mediterranean fever (FMF, OMIM no. 249100) is an inherited autoinflammatory
disorder resulting from MEFV gene mutations. A 15‑year‑old girl from Kerala, South India …
disorder resulting from MEFV gene mutations. A 15‑year‑old girl from Kerala, South India …
POS1334 OCULAR CICATRICIAL PEMPHIGOID: IS THERE AN ASSOCIATION WITH AUTOIMMUNE DISEASES?
A Ringer, AM Smichowski, R Gomez, BM Virasoro… - 2022 - ard.bmj.com
Background Ocular Cicatricial Pemphigoid (OCP) is an infrequent, systemic cicatricial
immune-mediated disease, belonging to the group of membranous-mucosal pemphigoids …
immune-mediated disease, belonging to the group of membranous-mucosal pemphigoids …