Mutations in the familial Mediterranean fever gene of patients with IgA nephropathy and other forms of glomerulonephritis
β Scribed by OL Kukuy; J Kopolovic; A Blau; A Ben-David; D Lotan; M Shaked; Y Shinar; D Dinour; P Langevitz; A Livneh
- Book ID
- 110888539
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 93 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0009-9163
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π SIMILAR VOLUMES
Familial Mediterranean fever (FMF) is an autosomal recessive disease clinically characterized by recurrent short self-limited attacks of fever accompanied by peritonitis, pleurisy, and arthritis and can lead to amyloidosis and renal failure in the longer term. It is prevalent mainly in non-Ashkenazi
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