familial

(redirected from familial Mediterranean fever)
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Synonyms for familial

of or relating to the family or household

Synonyms for familial

occurring among members of a family usually by heredity

References in periodicals archive ?
Evaluation of various cardiac autonomic indices in patients with familial Mediterranean fever on colchicine treatment.
Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever.
33) "International Study Group for Phenotype-Genotype Correlation in Familial Mediterranean Fever, Country as the primary risk factor for renal amyloidosis in FMF".
The eficacy of canakinumab in the treatment of a patient with familial Mediterranean fever and longstanding destructive arthritis.
Inflammatory/demyelinating central nervous system involvement in familial Mediterranean fever (FMF): coincidence or association?
Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations.
Frequency of alterations in the MEFV gene and clinical signs in familial Mediterranean fever in Central Anatolia, Turkey.
Korkmaz, "The frequency of sacroiliitis in familial Mediterranean fever and the role of HLA-B27 and MEFV mutations in the development of sacroiliitis," Clinical Rheumatology, vol.
1) about the early markers of atherosclerosis in patients with Familial Mediterranean Fever (FMF) by the measurements of serum paraoxonase-1 activity, mean platelet volume (MPV) and malondialdehyde level.
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent self-limited attacks of fever associated with serositis which usually involves the peritoneum, pleura, or synovium.
It is also an effective treatment for familial Mediterranean fever, a condition that affects about 100,000 people worldwide.
The most common periodic fever among humans is known as familial Mediterranean fever, affecting people of Mediterranean and Middle Eastern descent.
Familial mediterranean fever (FMF) is an autosomal recessively inherited disorder characterized by recurrent, inflammatory self limited episodes of fever and other symptoms.
Less common conditions include erythema multiforme, erythema nodusum, tuberculosis, leukemia cutis, lupus erythematosus, vasculitis, pyoderma gangrenosa, Behcet's disease, erythema elevatum diutinum, familial Mediterranean fever, and Sweet's syndrome.
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