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FMF50: a score for assessing outcome in familial Mediterranean fever

✍ Scribed by Ozen, S.; Demirkaya, E.; Duzova, A.; Erdogan, O.; Erken, E.; Gul, A.; Kasapcopur, O.; Kasifoglu, T.; Kisacik, B.; Ozdogan, H.; Tunca, M.; Acikel, C.; Direskeneli, H.; Basbozkurt, G.; Sayarlioglu, M.; Yuksel, S.; Yildiz, F.; Donmez, O.; Berdeli, A.; Senel, S.; Ayaz, N.; Polat, A.; Sozeri, B.; Tabel, Y.; Akar, S.; Onat, A.; Ozkaya, O.; Emre, S.; Akinci, N.; Ozcelik, G.; Yavuz, S.; Yesilkaya, S.; Ugurlu, S.; Gok, F.; Poyrazoglu, H.; Bakkaloglu, S.; Erten, S.; Tufan, A.; Goker, B.; Kavukcu, S.; Cakar, N.; Saldir, M.; Delibas, A.; Makay, B.; K saarslan, A.; Unsal, S.; Topaloglu, R.; Erdem, H.

Book ID
124079490
Publisher
BMJ Publishing Group
Year
2014
Tongue
English
Weight
539 KB
Volume
73
Category
Article
ISSN
0003-4967

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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