Informasjon, tilstand

Familiær middelhavsfeber

Familiær middelhavsfeber er en sjelden, arvelig sykdom som først og fremst oppstår i befolkningsgrupper fra områder rundt det indre Middelhavet.

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Referanser

  1. Herlin T, Sørensen N, Veirum J. Arvelige periodiske febersyndromer. Ugeskr Læger 2010 Oct 11 Epub ahead of print.
  2. Rosenberg PM, Goldfinger SE. Clinical manifestations and diagnosis of familial Mediterranean fever. UpToDate, last updated May 14, 2010. UpToDate
  3. Sohar E, Gafhi J, Pras M et al. Familial mediterranean fever. A survey of 470 cases and review of the literature. Am J Med 2007; 43: 227-53. PubMed
  4. The French FMF consortium. A candidate gene for familial Mediterranean fever. Nat Genet 1997; 17: 25-31. PubMed
  5. The International FMF consortium. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. Cell 1997: 90; 797-807.
  6. Sohar E, et al. Familial Mediterranean fever. A survey of 470 cases and review of the literature. Am J Med 1967; 43: 227. PubMed
  7. Lidar M, Yaqubov M, Zaks N, Ben-Horin S, Langevitz P, Livneh A. Clinical manifestations and diagnosis of familial Mediterranean fever. J Rheumatol 2006; 33: 1089-92. PubMed
  8. Ben-Chetrit E, Levy M. Familial Mediterranean Fever. Lancet 1998; 351: 659. PubMed
  9. Goldfinger SE. Colchicine for familial Mediterranean fever. N Engl J Med 1972; 287:1302. New England Journal of Medicine
  10. Roldan R, Ruiz AM, Miranda MD et al. Anakinra: new therapeutic approach in children with familial Mediterranean fever resistant to colchicine. Joint Bone Spine 2008; 75: 504-5. PubMed
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