Results 21 to 30 of about 35,452 (278)

Development of the autoinflammatory disease damage index (ADDI) [PDF]

open access: yes, 2016
OBJECTIVES: Autoinflammatory diseases cause systemic inflammation that can result in damage to multiple organs. A validated instrument is essential to quantify damage in individual patients and to compare disease outcomes in clinical studies.
Al-Mayouf, SM   +48 more
core   +14 more sources

A private hospital’s approach to treating acute familial Mediterranean fever in Dar es Salaam

open access: yesSAGE Open Medical Case Reports, 2023
Familial Mediterranean fever is a rare autosomal recessive autoinflammatory disorder prevalent in Middle Eastern populations, characterized by episodic abdominal pain. This case report presents a 34-year-old Egyptian man with severe lower abdominal pain,
Willbroad Kyejo   +8 more
doaj   +1 more source

Familial Mediterranean fever: issues of diagnosis and treatment

open access: yesЛечащий Врач, 2023
Familial Mediterranean fever is an autoinflammatory genetically determined autosomal recessive disease caused by a mutation of the MEFV gene. Familial Mediterranean fever is recorded mainly in populations of Middle Eastern origin, historically inhabiting
G. R. Bikbavova   +3 more
doaj   +1 more source

Real-Life Data From the Largest Pediatric Familial Mediterranean Fever Cohort

open access: yesFrontiers in Pediatrics, 2022
Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease manifesting phenotypic heterogeneity. It is a clinically diagnosed disease supported by MEditerranean FeVer (MEFV) gene mutation analysis.
Kübra Öztürk   +13 more
semanticscholar   +1 more source

Amyloidosis and Glomerular Diseases in Familial Mediterranean Fever

open access: yesMedicina, 2021
Familial Mediterranean fever (FMF) is a genetic autoinflammatory disease with autosomal recessive transmission, characterized by periodic fever attacks with self-limited serositis.
Rossella Siligato   +4 more
semanticscholar   +1 more source

A case report of a boy suffering from type 1 diabetes mellitus and familial Mediterranean fever

open access: yesItalian Journal of Pediatrics, 2021
Background Type 1 diabetes mellitus could be associated with other autoimmune diseases, such as autoimmune thyroid disease, celiac disease, but the association with Familial Mediterranean Fever is rare, we describe a case of a boy with type 1 Diabetes ...
Maria Francesca Gicchino   +4 more
doaj   +1 more source

Concurrence of familial Mediterranean fever and Behçet’s disease: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2023
Background Familial Mediterranean fever and Behçet’s disease are distinct disorders that are prevalent in the Mediterranean and Middle Eastern populations.
Adhora Mir   +2 more
doaj   +1 more source

Familial Mediterranean fever-related miR-197-3p targets IL1R1 gene and modulates inflammation in monocytes and synovial fibroblasts

open access: yesScientific Reports, 2021
Familial Mediterranean fever (FMF); is an autosomal recessively inherited autoinflammatory disease caused by the mutations in the Mediterranean Fever ( MEFV ) gene.
Yeliz Z. Akkaya-Ulum   +6 more
semanticscholar   +1 more source

Familial Mediterranean fever may mimic acute appendicitis in children

open access: yesPediatric surgery international (Print), 2022
Acute appendicitis is the most common surgical emergency in children. Diagnosis and management are often straightforward. However, familial Mediterranean fever is an important condition to consider in the assessment of children with acute abdominal pain,
P. Wekell, T. Wester
semanticscholar   +1 more source

Evaluation of Cardiac Arrhythmia Susceptibility in Pediatric Familial Mediterranean Fever Patients

open access: yesJournal of Contemporary Medicine, 2023
Aim: Familial Mediterranean fever is an autoinflammatory disease characterized by attacks of inflammation. Despite treatment, there is evidence of subclinical persistence of inflammation with normal laboratory values.
Şükrü  Arslan   +2 more
doaj   +1 more source

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