Application of the new pediatric criteria and Tel Hashomer criteria in heterozygous patients with clinical features of FMF

Author:

Özçakar Z. Birsin,Yalçınkaya Fatoş,Çakar Nilgün,Acar Banu,Bilgiç A. Evren,Uncu Nermin,Kara Nazlı,Ekim Mesiha,Kasapçopur Özgür

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Akar N, Misiroglu M, Yalcinkaya F et al (2000) MEFV mutations in Turkish patients suffering from familial Mediterranean fever. Hum Mutat 15:118–119

2. Armenian HK (1982) Genetic and environmental factors in etiology of familial paroxysmal polyserositis. An analysis of 150 cases from Lebanon. Trop Geogr Med 34:183–187

3. Ben-Chetrit E, Levy M (1998) Familial Mediterranean fever. Lancet 351:659–664

4. Ben-Chetrit E, Urieli-Shoval S, Calko S, Abeliovich D, Matzner Y (2002) Molecular diagnosis of FMF: lessons from a study of 446 unrelated individuals. Clin Exp Rheumatol 20:25–29

5. Jarjour RA (2010) Familial Mediterranean fever in Syrian patients: MEFV gene mutations and genotype–phenotype correlation. Mol Biol Rep 37:1–5

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