Frequencies of the MEFV Gene Mutations in Azerbaijan
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References
- Habahbeh LA, Hiary MA, Zaben SF, Al-Momanu A, Khawawneh R, Mallouh MA, et al. Genetic profile of patients with Familial Mediterranean Fever (FMF): Single cenger experience at King Hussein Medical Center KHMC). Med Arch. 2015; 69(6): 417–420.
- Ozen S, Batu ED. The myths we believed in familial Mediterranean fever: What have we learned in the past years. Semin Immunopathol. 2015; 37(4): 363–639.
- Rigante D, Frediani B, Cantarini L. A comprehensive overview of the hereditary periodic fever syndromes. Clin Rev Allergy Immunol. 2018; 54(3): 446–453.
- Anwar GM, Fouad HM, Abd El-Hamid A, Mahmoud F, Musa N, Lotfi H, et al. A study of familial Mediterranean Fever (MEFV) gene mutations in Egyptian children with type 1 diabetes mellitus. Eur J Med Genet. 2015; 58(1): 31–34.
- Beheshtian M, Izadi N, Kriegshauser G, Kahrizi K, Mehr EP, Rostami M, et al. Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations. J Genet. 2016; 95(3): 667–674.
- Debeljak M, Toplak N, Abazi N, Szabados B, Mulaosmanović V, Radović J, et al. The carrier rate and spectrum of MEFV gene mutations in central and southeastern European populations. Clin Exp Rheumatol. 2015; 33(6 Suppl 94): S19–S23.
- Wu B, Xu T, Li Y, Yin X. Interventions for reducing inflammation in familial Mediterranean fever. Cochrane Database Syst Rev. 2018; 10(10): CD010893.
- Yates AD, Achuthan P, Akanni W, Allen J, Allen J, Alvaarez-Jarreta J, et al. Ensembl 2020. Nucleic Acids Res. 2020; 48(D1): D682–D688.
- Milenković J, Vojinović J, Debeljak M, Toplak N, Lazarević D, Avčin T, et al. Distribution of MEFV gene mutations and R202Q polymorphism in the Serbian population and their influence on oxidative stress and clinical manifestations of inflammation. Pediatr Rheumatol Online J. 2016; 14(1):39.
- Yaşar Bilge Ş, Sarı İ, Solmaz D, Şenel S, Emmungil H, Kılıç L, et al. The distribution of MEFV mutations in Turkish FMF patients: Multicenter study representing results of Anatolia. J Med Sci. 2019; 49(2): 472–477.
- Yilmaz G, Senes M, Kayalp D, Yucel D. Is Turkish MEFV mutations spectrum different among regions?. J Clin Lab Anal. 2016; 30(5):641–644.
- Zerkaoui M, Laarabi FZ, Ajhoun Y, Chkirate B, Sefiani A. A novel single variant in the MEFV gene causing Mediterranean fever and Behçet's disease: A case report. J Med Case Rep. 2018; 12(1): 53.
- Huseynova LS, Aiyeva KA, Najafzada GB, Yusufova KhJ, Hashimova AR. Molecular-genetic research of MEFV gene in population of Azerbaijan Republic. Poland Sylwan. 2018; 162(5):31–36.
- Rigante D. A developing portrait of hereditary periodic fevers in childhood. Expert Opin Orphan Drugs. 2018; 6(1): 47–55.
- Fragouli E, Eliopoulos E, Petraki E, Sidiropoulos P, Aksentijevich I, Galanakis E, et al. Familial Mediterranean fever in Crete: A genetic and structural biological approach in a population of ‘intermediate risk.’ Clin Genet. 2008; 73(2): 152–159.
- Jalkh N, Genin E, Chouery E, Delague V, Medlej-Hashim M, Idrac C-A, et al. Familial Mediterranean fever in Lebanon: founder effects for different MEFV mutations. Ann Hum Genet. 2008; 72(10): 41–47.
- Bonyadi M, Esmaeili M, Jalali H, Somi MH, Ghaffari A, Rafeey M, et al. MEFV mutations in Iranian Azeri Turkish patients with familial Mediterranean fever. Clin Genet. 2009; 76(11): 477–480.
- Otsuka M, Koga T, Sumiyoshi R, Koike Y, Furukawa K, Okamoto M, et al. A case of neutrophilic dermatosis with MEFV gene variant and abnormal activation of peripheral blood monocytes: A case report. Immun Med. 2019; 42(6): 45–49.
- Berg JS, Adams M, Nassar N, Bizon C, Lee K, Schmitt CP, et al. An informatics approach to analyzing the incidentalome. Genet Med. 2013; 15(1): 36–44.
- Masters SL, Lagou V, Jeru I, Baker PJ, Van Eyck L, Parry DA, et al. Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation. Sci Transl Med. 2016; 8: 332–345.
- Kiyota M, Oya M, Ayano M, Niiro H, Iwasaki T, Fujiwara M, et al. First case of pyrin-associated autoinflammation with neutrophilic dermatosis complicated by amyloidosis. Rheumatology (Oxford). 2020; 59(9): e.41–e43.
- Moghaddas F, Llamas R, De Nardo D, Martinez-Banaclocha H, Martinez-Garcia JJ, Mesa-del-Castillo P, et al. A novel pyrin-associated autoinflammation with neu-trophilic dermatosis mutation further defines 14-3-3 binding of pyrin and distinction to familial Mediterranean fever. Ann Rheum Dis. 2017; 76(12): 2085–2094.
- Grossman C, Kassel Y, Livneh A, Ben-Zvi I. Familial Mediterranean fever (FMF) phenotype in patients homozygous to the MEFV M694V mutation. Eur J Med Genet. 2019; 62(6): 103532.
- Mattit H, Joma M, Al-Cheikh S, El-Khateeb M, Medlej-Hashin M, Salem N, et al. Familial Mediterranean fever in the Syrian population: Gene mutation frequencies, carrier rates and phenotype-genotype correlation. Eur J Med Genet. 2006; 49(6): 481–486.
- Jarjour RA. Familial Mediterranean fever in Syrian patients: MEFV gene mutations and genotype-phenotype correlation. Mol Biol Rep. 2010; 37(1): 1–5.
- Jarjour RA, Dodaki R. Arthritis patterns in familial Mediterranean fever patients and association with M694V mutation. Mol Biol Rep. 2011; 38(3): 2033–2036.
DOI: https://doi.org/10.2478/bjmg-2021-0017 | Journal eISSN: 2199-5761
Language: English
Page range: 33 - 38
Published on: Jun 5, 2022
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
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© 2022 LS Huseynova, SN Mammadova, KAA Aliyeva, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.