Evaluation of clinical concordance in FMF siblings with identical biallelic exon 10 variants
- 17 February 2026
- journal article
- research article
- Published by Taylor & Francis in Postgraduate Medicine
- Vol. 138 (2) , 250-256
Abstract
The most prevalent monogenic autoinflammatory disease, familial Mediterranean fever (FMF), is characterized by repeated, self-limiting flare-ups of fever, serositis, and arthritis [1]. The disease ...Keywords
This publication has 25 references indexed in Scilit:
- Different arthritis patterns in pediatric familial Mediterranean fever: Focus on exon 10 biallelic pathogenic genotypesJoint Bone Spine, 2025
- Preliminary Evaluation for the Development of a Scoring System to Predict Homozygous M694V Genotype in Familial Mediterranean Fever PatientsJCR: Journal of Clinical Rheumatology, 2025
- Physical fitness in adolescent patients with familial Mediterranean feverRheumatology International, 2024
- Experimental models in Familial Mediterranean Fever (FMF): Insights into pathophysiology and therapeutic strategiesExperimental and Molecular Pathology, 2024
- Familial Mediterranean Fever: How to Interpret Genetic Results? How to Treat? A Quarter of a Century After the Association with the Mefv GeneCurrent Rheumatology Reports, 2022
- Sex and gender: modifiers of health, disease, and medicineThe Lancet, 2020
- Sex Differences in Pediatric RheumatologyClinical Reviews in Allergy & Immunology, 2017
- ‘Silent’ carriage of two familial Mediterranean fever gene mutations in large families with only a single identified patientClinical Genetics, 2011
- A new set of criteria for the diagnosis of familial Mediterranean fever in childhoodRheumatology, 2009
- Long‐term colchicine treatment in children with familial mediterranean feverArthritis & Rheumatism, 1991