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Year 2014, Volume: 19 Issue: 4, 198 - 201, 23.03.2015

Abstract

References

  • Shinar Y, Livneh A, Villa Y, et al. Common mutations in the familial Mediterranean fever gene associate with rapid progression to disability in non-Ashkenazi Jewish multiple sclerosis patients. Genes Immun 2003; 4: 197-203.
  • Schwartz T, Langevitz P, Zemer D, et al. Behçet's disease in Familial Mediterranean fever: characterization of the association between the two diseases. Semin Arthritis Rheum 2000; 29: 286-295.
  • Livneh A, Aksentijevich I, Langevitz P, et al. A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMF-BD). Eur J Hum Genet 2006; 9: 191-196.
  • Rabinovich E, Shinar Y, Leiba M, et al. Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis. Scand J Rheumatol 2007; 36: 48-52.
  • Imirzalioglu N, Dursun A, Tastan B, Soysal Y, Yakicier MC. MEFV gene is a probable susceptibility gene for Behçet's disease. Scand J Rheumatol 2005; 34: 56-58.
  • Karabudak R, Dogulu CF, Nurlu G, Simsek H, Saatci I. Central nervous system demyelination in familial Mediterranean fever: is it a coincidence? Eur J Neurol 2003; 10: 327-328.

CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION

Year 2014, Volume: 19 Issue: 4, 198 - 201, 23.03.2015

Abstract

Familial Mediterranean Fever (FMF) is a hereditary disease seen mainly around the Mediterranean. The most common mutations are M694V, M680I, V726A and E148. Neurological findings and magnetic resonance imaging (MRI) abnormalities resembling multiple sclerosis have been reported in very few cases. We present a case where an M694V mutation was found together with familial Mediterranean fever and multiple sclerosis-type demyelinizing disease as this combination is rarely seen.

References

  • Shinar Y, Livneh A, Villa Y, et al. Common mutations in the familial Mediterranean fever gene associate with rapid progression to disability in non-Ashkenazi Jewish multiple sclerosis patients. Genes Immun 2003; 4: 197-203.
  • Schwartz T, Langevitz P, Zemer D, et al. Behçet's disease in Familial Mediterranean fever: characterization of the association between the two diseases. Semin Arthritis Rheum 2000; 29: 286-295.
  • Livneh A, Aksentijevich I, Langevitz P, et al. A single mutated MEFV allele in Israeli patients suffering from familial Mediterranean fever and Behçet's disease (FMF-BD). Eur J Hum Genet 2006; 9: 191-196.
  • Rabinovich E, Shinar Y, Leiba M, et al. Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis. Scand J Rheumatol 2007; 36: 48-52.
  • Imirzalioglu N, Dursun A, Tastan B, Soysal Y, Yakicier MC. MEFV gene is a probable susceptibility gene for Behçet's disease. Scand J Rheumatol 2005; 34: 56-58.
  • Karabudak R, Dogulu CF, Nurlu G, Simsek H, Saatci I. Central nervous system demyelination in familial Mediterranean fever: is it a coincidence? Eur J Neurol 2003; 10: 327-328.
There are 6 citations in total.

Details

Primary Language English
Journal Section Case Report
Authors

Adile Ozkan

Sule Kosar This is me

Ahmet Uludag

Mete Hazinedaroglu This is me

Handan İsin Ozisik Karaman This is me

Publication Date March 23, 2015
Published in Issue Year 2014 Volume: 19 Issue: 4

Cite

APA Ozkan, A., Kosar, S., Uludag, A., Hazinedaroglu, M., et al. (2015). CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION. EASTERN JOURNAL OF MEDICINE, 19(4), 198-201.
AMA Ozkan A, Kosar S, Uludag A, Hazinedaroglu M, Ozisik Karaman Hİ. CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION. EASTERN JOURNAL OF MEDICINE. March 2015;19(4):198-201.
Chicago Ozkan, Adile, Sule Kosar, Ahmet Uludag, Mete Hazinedaroglu, and Handan İsin Ozisik Karaman. “CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION”. EASTERN JOURNAL OF MEDICINE 19, no. 4 (March 2015): 198-201.
EndNote Ozkan A, Kosar S, Uludag A, Hazinedaroglu M, Ozisik Karaman Hİ (March 1, 2015) CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION. EASTERN JOURNAL OF MEDICINE 19 4 198–201.
IEEE A. Ozkan, S. Kosar, A. Uludag, M. Hazinedaroglu, and H. İ. Ozisik Karaman, “CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION”, EASTERN JOURNAL OF MEDICINE, vol. 19, no. 4, pp. 198–201, 2015.
ISNAD Ozkan, Adile et al. “CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION”. EASTERN JOURNAL OF MEDICINE 19/4 (March 2015), 198-201.
JAMA Ozkan A, Kosar S, Uludag A, Hazinedaroglu M, Ozisik Karaman Hİ. CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION. EASTERN JOURNAL OF MEDICINE. 2015;19:198–201.
MLA Ozkan, Adile et al. “CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION”. EASTERN JOURNAL OF MEDICINE, vol. 19, no. 4, 2015, pp. 198-01.
Vancouver Ozkan A, Kosar S, Uludag A, Hazinedaroglu M, Ozisik Karaman Hİ. CONCURRENT DEMYELINIZING CENTRAL NERVOUS SYSTEM INVOLVEMENT IN A CASE OF FAMILIAL MEDITERRANEAN FEVER WITH THE M694V MUTATION. EASTERN JOURNAL OF MEDICINE. 2015;19(4):198-201.