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First Genetically Confirmed Case of Familial Mediterranean Fever in Somalia: A Case Report and Diagnostic Challenges in Resource-Limited Setting. [PDF]
Int Med Case Rep JJama MA +4 more
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Familial Mediterranean Fever Intertwined With a Diagnosis of Crohn's Disease: A Case Report. [PDF]
CureusFerreira C +3 more
europepmc +1 more source
Familial Mediterranean fever with massive recurrent ascites: A case report.
The Turkish Journal of Gastroenterology, 2003 Ayhan Hilmi ÇEKİN +4 more
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Correction to: Expanding the Spectrum: a case of Giant cell arteritis encountered in familial Mediterranean fever. [PDF]
Oxf Med Case Reportseuropepmc +1 more source
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Lancet, The, 1998
A 33-year-old moderately mentally handicapped man who was living in a group home presented to our clinic with a 1-week history of pain, swelling, and erythema of the lower portion of the right leg and foot. The patient was of Roman Catholic, Italian origin, although the history of his distant family revealed that some of his relatives had emigrated ...
Eldad Ben-Chetrit, Micha Levy
exaly +5 more sources
A 33-year-old moderately mentally handicapped man who was living in a group home presented to our clinic with a 1-week history of pain, swelling, and erythema of the lower portion of the right leg and foot. The patient was of Roman Catholic, Italian origin, although the history of his distant family revealed that some of his relatives had emigrated ...
Eldad Ben-Chetrit, Micha Levy
exaly +5 more sources
French protocol for the diagnosis and management of familial Mediterranean fever.
La Revue de medecine interne, 2023Familial Mediterranean fever is the most common monogenic auto-inflammatory disease in the world. It mainly affects people originating from the Mediterranean region. The mutated gene is MEFV, which codes for pyrin.
S. Georgin-lavialle +11 more
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[Familial Mediterranean fever in 2020].
Néphrologie & Thérapeutique, 2021Familial Mediterranean fever is the most frequent autoinflammatory disease with autosomal recessive transmission. Most patients carry mutations in the MEFV gene encoding the protein marenostrin/pyrin. It is characterised by short ant recurrent attacks of
L. Savey +2 more
semanticscholar +1 more source
Archives of Internal Medicine, 1958
I. Introduction The purpose of this communication is to describe a disease which we define as a heredofamilial syndrome of undetermined pathogenesis in persons of Mediterranean stock, becoming manifest as a rule in infancy or adolescence and characterized by short recurrent bouts of fever accompanied by pain in the abdomen or chest or one or multiple ...
H, HELLER, E, SOHAR, L, SHERF
openaire +2 more sources
I. Introduction The purpose of this communication is to describe a disease which we define as a heredofamilial syndrome of undetermined pathogenesis in persons of Mediterranean stock, becoming manifest as a rule in infancy or adolescence and characterized by short recurrent bouts of fever accompanied by pain in the abdomen or chest or one or multiple ...
H, HELLER, E, SOHAR, L, SHERF
openaire +2 more sources
Current Opinion in Rheumatology, 2016
Purpose of review Familial Mediterranean fever (FMF) is the oldest and most common of the hereditary autoinflammatory diseases (AIDs). A large body of information has been accumulated over recent years on the pathophysiology, diagnosis and treatment of these diseases. The purpose of this review is to bring an up-to-date summary
Shai, Padeh, Yackov, Berkun
openaire +2 more sources
Purpose of review Familial Mediterranean fever (FMF) is the oldest and most common of the hereditary autoinflammatory diseases (AIDs). A large body of information has been accumulated over recent years on the pathophysiology, diagnosis and treatment of these diseases. The purpose of this review is to bring an up-to-date summary
Shai, Padeh, Yackov, Berkun
openaire +2 more sources