Screening for inherited metabolic disorders in patients with Familial Mediterranean Fever

نویسندگان

  • E Kiykim
  • AC Aktuglu-Zeybek
  • K Barut
  • T Zubarioglu
  • MS Cansever
  • A Aydin
  • O Kasapcopur
چکیده

Introduction Familial Mediterranean fever (FMF) is an autosomal recessive auto-inflammatory disease, presenting with recurrent episodes of fever and polyserositis. Diagnosis of FMF is may be challenging especially in pediatric population. Mitochondrial fatty acid oxidation disorders and porphyrias can present with periodic abdominal and muscle pain. Incidence of both FMF and inherited metabolic disorders (IMD) are increased in Turkish patients partially due to high consanguinity rates.

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Familial Mediterranean Fever: Review of Literature and Report of Two Cases

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عنوان ژورنال:

دوره 13  شماره 

صفحات  -

تاریخ انتشار 2015