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A comparison of clinical findings of familial Mediterranean fever patients with and without amyloidosis

✍ Scribed by Ayse Cefle; Sevıl Kamali; Mehmet Sayarlioglu; Murat Inanc; Lale Ocal; Orhan Aral; Meral Konice; Ahmet Gul


Publisher
Springer
Year
2004
Tongue
English
Weight
184 KB
Volume
25
Category
Article
ISSN
0172-8172

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Familial Mediterranean fever (FMF) is an autosomal recessively inherited disease affecting patients of the Mediterranean basin. FMF is characterized by recurrent episodes of fever accompanied with topical signs of inflammation. Some patients can develop a renal amyloidosis associated (AA) amyloidosi