Results 61 to 70 of about 846,391 (207)

Familial mediterranean fever and immunoglobulin A nephropathy: A case report and review of the literature

Saudi Journal of Kidney Diseases and Transplantation, 2020
Familial Mediterranean fever (FMF) is an autosomal recessive disease charac-terized by recurrent fever episodes and polyserositis. The most important complication is amyloidosis. Nonamyloidotic nephropathy in FMF is poorly documented. Besides amyloidosis,
Fatih Yılmaz, Meryem Keleş
doaj   +1 more source

Exploring Diagnostic Challenges: A Case Report Commentary on “Solving a Diagnostic Dilemma in a Patient With Periodic Fever—When the Pieces of the Puzzle Finally Fit”

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT This case highlights the diagnostic challenge of distinguishing periodic fever syndromes with prominent neurological features from interferonopathies. While the absence of specific features on MRI/MRA and SAVI reduces the likelihood of certain subtypes, genetic evaluation involving interferon pathway genes remains important.
Fatih Kelesoglu, Adem Polat
wiley   +1 more source

Familial Mediterranean fever in northwest of Iran (Ardabil): The first global report from Iran [PDF]

Familial Mediterranean fever (FMF), which is the prototype of the hereditary periodic fever syndromes, is common in the countries around the Mediterranean Sea. Considering its geographical position in the northwest of Iran, with its population of Turkish
فیضی, ایرج, خلفی, جعفر, صالح زاده, فرهاد, عظیمی, هرمز, ذولفقاری, علی اصغر, براک, منوچهر, جستان, مارینا, حبیب زاده, شهرام, امامی, دینا, یزدانبد, عباس, بشردوست, بهمن   +10 more
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38-year-old woman with recurrent abdominal pain, but no fever

International Journal of General Medicine, 2012
Kentaro Iwata1, Tomoko Toma2, Akihiro Yachie21Department of Infectious Diseases, Kobe University Hospital, Kobe, Japan; 2Department of Pediatrics, Graduate School of Medical Science and School of Medicine, Kanazawa University, Kanazawa, JapanAbstract: A ...
Iwata K, Toma T, Yachie A
doaj  

A Narrative Review on Integrative Bioinformatics Approaches for microRNA Research in Familial Mediterranean Fever: Current Insights and Future Directions

Health Science Reports, Volume 9, Issue 3, March 2026.
ABSTRACT Background and Aims Familial Mediterranean Fever (FMF) is a monogenic autoinflammatory disease caused by mutations in the MEFV gene, resulting in recurrent inflammatory episodes and a risk of developing amyloidosis. Although its pathophysiology is well described, FMF still lacks specific biomarkers and personalized treatment strategies ...
Zeinab Skaineh, Razane Hammoud, Ahlam Chaaban, Eliana Eldawra, José‐Noel Ibrahim   +4 more
wiley   +1 more source

Comparison of Different Pharmaceutical Preparations of Colchicine in Children with Familial Mediterranean Fever: Is Colchicine Opocalcium a Good Alternative?

, 2021
Background: Colchicine is an anti-inflammatory agent used for preventing familial Mediterranean fever (FMF) attacks and amyloidosis.
Selçuk Yüksel, Unsal, Erbil, Serkan Türkuçar, Makay, BALAHAN, Acari, Ceyhun, Balahan Makay, Yukser, Selcuk, Yuksel, Selcuk, Ceyhun Acari, Gülçin Otar Yener, Erbil Ünsal, Turkucar, Serkan, Yener, Gulcin Otar, Hatice Adıgüzel Dundar, Dundar, Hatice Adiguzel   +14 more
core   +1 more source

Natural‐History Mapping of Lysosomal Storage Disorders (LSDs): Gaucher Disease as a Model for Precision Care

Journal of Inherited Metabolic Disease, Volume 49, Issue 1, January 2026.
ABSTRACT Natural‐history datasets have become pivotal for drug development and for shaping clinical‐practice guidelines in rare diseases, yet many lysosomal storage disorders would benefit from deep phenotyping and modern analytic methods. Our objective was to integrate the past decade of genomic, cellular, treatment‐outcome, and regulatory advances ...
Noor Ul Ain, Maya Vaishnaw, Pramod. K. Mistry   +2 more
wiley   +1 more source

DAPSONE AS AN ALTERNATIVE THERAPY IN CHILDREN WITH FAMILIAL MEDITERRANEAN FEVER [PDF]

Objective: Familial Mediterranan Fever is an hereditary autoinflammatory disease that presents with recurrent febrile attacks and poly serositis. Colchicine is the only known treatment in this diease.
صالح زاده, فرهاد, جهانگیری, سپیده, محمدی کلاسرلو, ایلنار   +2 more
core  

Familial Mediterranean Fever

, 2015
Familial Mediterranean Fever (FMF) is an autosomal recessive hereditary disease that affects mainly the people of Jewish, Arabic, Turkish, and Armenian origins.
Yilmaz, Yunus, Ustebay, Sefer, Ustebay, DÖNDÜ ÜLKER   +2 more
core   +1 more source

Musculoskeletal manifestations occur predominantly in patients with later-onset familial Mediterranean fever: Data from a multicenter, prospective national cohort study in Japan [PDF]

, 2018
BACKGROUND: We showed previously that Japanese individuals with familial Mediterranean fever (FMF) have a more atypical phenotype compared to endemic areas.
Ayuko Takatani (4003193), Akihiro Yachie (739217), Igawa, Takashi, Fujita, Yuya, Midori Ishida, Kiyoshi Migita (290200), Iwamoto, Naoki, Yuya Fujita (5997464), Hideki Nakamura, Takashi Igawa, Ayako Nishino (4003187), Umeda, Masataka, Atsushi Kawakami (398370), Tsuji, Sosuke, Kazunaga Agematsu (398352), Tomoki Origuchi, Shin-ya Kawashiri (4003199), Sumiyoshi, Remi, Hideki Nakamura (1543762), Kawashiri, Shin-ya, Tomoki Origuchi (739149), Ayuko Takatani, Kiyoshi Migita, Yuya Fujita, Junya Masumoto, Takatani, Ayuko, Tomohiro Koga (398369), Ishida, Midori, Ayako Nishino, Agematsu, Kazunaga, Junya Masumoto (277060), Atsushi Kawakami, Naoki Iwamoto, Kunihiro Ichinose (4003172), Toshimasa Shimizu, Shoichi Fukui, Sosuke Tsuji (4003196), Shin-ya Kawashiri, Kawakami, Atsushi, Shimizu, Toshimasa, Remi Sumiyoshi, Masumoto, Junya, Akihiro Yachie, Remi Sumiyoshi (5997467), Koga, Tomohiro, Tamai, Mami, Shoichi Fukui (4003181), Masataka Umeda, Nishino, Ayako, Midori Ishida (5997461), Naoki Iwamoto (4003208), Yushiro Endo, Endo, Yushiro, Mami Tamai (4003175), Tomohiro Koga, Toshimasa Shimizu (4003184), Masataka Umeda (1543771), Yushiro Endo (5997458), Mami Tamai, Migita, Kiyoshi, Sosuke Tsuji, Kazunaga Agematsu, Origuchi, Tomoki, 遠藤, 友志郎, Fukui, Shoichi, Takashi Igawa (5700311), Nakamura, Hideki, Yachie, Akihiro, Ichinose, Kunihiro, Kunihiro Ichinose   +69 more
core   +1 more source