Do the MEFV gene mutations increase in patients with autosomal dominant polycystic kidney disease? Preliminary analysis

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DOĞAN İ., Altunoglu A., Ozturk C., Kose K., Yuces G., ERSOY O., ...Daha Fazla

ANNALS OF CLINICAL AND ANALYTICAL MEDICINE, cilt.11, sa.4, ss.311-313, 2020 (ESCI)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 11 Sayı: 4
  • Basım Tarihi: 2020
  • Doi Numarası: 10.4328/acam.20053
  • Dergi Adı: ANNALS OF CLINICAL AND ANALYTICAL MEDICINE
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI)
  • Sayfa Sayıları: ss.311-313
  • Anahtar Kelimeler: Autosomal Dominant Polycystic Kidney Disease, Familial Mediterranean Fever, MEFV Gene Mutation, Colchicine, Amyloidosis, FAMILIAL MEDITERRANEAN FEVER, DIAGNOSIS, COEXISTENCE, AMYLOIDOSIS, CRITERIA
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Ankara Üniversitesi Adresli: Evet

Özet

Aim: The aim of the present study was to evaluate the frequency of MEFV gene mutations in autosomal dominant polycystic kidney disease (ADPKD) patients with abdominal pain, tenderness, fever or arthritis attacks who may have coexistence of Familial Mediterranean Fever (FMF).