A microscopic study of kidney tissue in familial mediterranean fever patients
✍ Scribed by Seda M. Sarı Kılıçaslan; Cevat Ayvalı; Hakkı Taştan
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 459 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0263-6484
- DOI
- 10.1002/cbf.1286
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✦ Synopsis
Abstract
Familial Mediterranean Fever (FMF) is an autosomal recessive hereditary disease leading mostly to renal failure and nephrotic syndrome. The ultrastructure of kidney has not been fully investigated in FMF associated renal disease. The aim of this study is to provide further evidence on the ultrastructure of kidney in patients with FMF who suffer from renal disease. Renal biopsies obtained from two patients who were diagnosed with FMF renal disease complications were examined. Examination of renal tissue by light and electron microscopy identified degenerations both in tubules and the filtration barrier. Foot processes were partly effaced. Amorphous material was found in thickened glomerular basement membranes. Fibrous material deposits in thick Bowman's capsule wall were also seen. Finally, degeneration in the form of folding of plasma membrane and vacuolization as well as fusion in mitochondria cristae, was observed. Accumulation of tissue remnants in the lumen was also found in tubules. Copyright © 2005 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
Familial Mediterranean fever is an autosomal recessive disorder characterised by episodic fever, abdominal and pleuritic pain, serositis and arthritis. The FMF gene (MEFV) has been mapped to chromosome 16p13.3 and generates a protein found exclusively in granulocytes. Seventeen mutations have been r
## Abstract ## Objective To define the frequency of the R92Q tumor necrosis factor receptor–associated periodic syndrome (TRAPS) mutation in patients with familial Mediterranean fever (FMF) and to study the role of this mutation in FMF. ## Methods Ninety‐two FMF patients and 250 controls were ge