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Incidence of familial Mediterranean fever (FMF) mutations among children of Mediterranean extraction with functional abdominal pain

✍ Scribed by Riva Brik; Dianna Litmanovitz; Drora Berkowitz; Raanan Shamir; Eldad Rosenthal; Marwan Shinawi; Ruth Gershoni-Baruch


Book ID
117847727
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
62 KB
Volume
138
Category
Article
ISSN
1097-6833

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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