Amyloidosis due to familial Mediterranean fever: clinical and laboratory findings in 51 patients

Cetinkaya, R; Odabas, AR; Selcuk, Y; Albayrak, Fatih

doi:10.1163/156856903767650880

Makale Tam Makale Uluslararası 2003

Amyloidosis due to familial Mediterranean fever: clinical and laboratory findings in 51 patients

R Cetinkaya, AR Odabas, Y Selcuk, Fatih Albayrak

PAIN CLINIC Cilt 15 · Sayı 3 · ss. 333–337 · 01.01.2003

DOI ile aç

Özet

Background: Familial Mediterranean fever (FMF) is a genetic multisystem disease, characterised by recurrent episodes of fever, peritonitis, pleuritis and arthritis. The most dangereous complication of the FMF is amyloidosis leading to end stage renal disease. The purpose of this study was to evaluate clinical and laboratory characteristics of patients with amyloidos due to FMF.

Atıf için künye

Cetinkaya, R., Odabas, A., Selcuk, Y., & Albayrak, F. (2003). Amyloidosis due to familial Mediterranean fever: clinical and laboratory findings in 51 patients. PAIN CLINIC, 15(3), 333–337. https://doi.org/10.1163/156856903767650880

BibTeX

@article{cetinkaya2003-228082,
  author = {Cetinkaya, R and Odabas, AR and Selcuk, Y and Albayrak, Fatih},
  title = {Amyloidosis due to familial Mediterranean fever: clinical and laboratory findings in 51 patients},
  journal = {PAIN CLINIC},
  year = {2003},
  volume = {15},
  number = {3},
  pages = {333--337},
  issn = {0169-1112},
  doi = {10.1163/156856903767650880},
  url = {https://akademik.atauni.edu.tr/yayinlar/228082-amyloidosis-due-to-familial-mediterranean-fever-clinical-and-laboratory-findings}
}