Relationship between clinical findings and genetic mutations in patients with familial Mediterranean fever
- Ayse Kilic1Email author,
- Muhammet Ali Varkal1,
- Mehmet Sait Durmus1,
- Ismail Yildiz1,
- Zeynep Nagihan Yürük Yıldırım2,
- Gorkem Turunc3,
- Fatma Oguz4,
- Mujgan Sidal1,
- Rukiye Eker Omeroglu5,
- Sevinc Emre5,
- Yasin Yilmaz3,
- Fatih Mehmet Kelesoglu5,
- Genco Ali Gencay3,
- Sonay Temurhan6,
- Filiz Aydin6 and
- Emin Unuvar1
© Kilic et al. 2015
Received: 25 August 2015
Accepted: 11 December 2015
Published: 12 December 2015
Familial Mediterranean fever (FMF) is one of the most frequent genetic diseases encountered in the Mediterranean region. We aimed to investigate the correlation between genetic mutations and the clinical findings in 562 patients with FMF.
In this retrospective cross-sectional study conducted with patients’ files between 2006, and 2013, reverse hybridization assay for MEFV gene mutations was used and the 12 most frequent mutations were screened. Mutation types and clinical findings were compared with variance analysis.
The mean age was 6.9 ± 3.4 years (range, 1.8-11.6 years). The most common symptom was fever (97.3 %). Thirty-four of the patients (6.04 %) were admitted with periodic fever only. Of these patients, M694V was the most common mutation type (73.5 %). The percentage of the patients predominantly presenting with recurrent abdominal pain was 77.78 % and the most frequent mutations were M694V and E148Q. The rate of arthritis and arthralgia was significantly higher in patients with M694V and E148Q mutations. Chest pain was reported more often in patients homozygous for M694V (61.4 %). Pericardial effusion was documented in the echocardiography of 10.9 % of the 229 children with chest pain. Some patients had both FMF and Henoch Schönlein purpura (HSP), and were more likely to harbor either homozygote M694V or E148Q mutations. The frequency of episodes was higher in patients with homozygous M694V mutations (number of attacks = 4.4 ± 1.6/month). Proteinuria was detected in 106 patients of cases (29.2 %), at an average of 854 ± 145 mg/L. Most of the patients with proteinuria and elevated serum amyloid-A had homozygous M694V mutation.
The most common mutation in children in Turkey with FMF is the M694V mutation. Recurrent abdominal pain, arthritis or arthralgia, chest pain, and pericarditis were commonly seen in patients with M694V and E148Q mutations.
The most noticable finding of the disease is painful febrile episodes accompanied by peritonitis, pleuritic pain or acute synovitis in many patients. Headache or diffuse myalgia and malaise can also occur. The acute phase reactants like serum amyloid A (SAA) are significantly elevated [4, 5]. Recurrent orchitis and meningitis are uncommon presentations.
In trials conducted in Turkish population, the most common mutations were reported as M694V, E148Q, M680I and V726A . The last ten years have seen much research into the effect of particular genetic mutations on clinical findings .
In this study, we aimed to investigate the correlation between genetic mutations and clinical findings on admission of 562 patients with recurrent fever, abdominal pain and/or arthritis/arthralgia and subsequently diagnosed as having FMF. The relationship between genetic mutations, types and the severity of clinical findings in patients who were diagnosed as having FMF were analyzed. Furthermore, the relationship between frequency of proteinuria and genetic mutations were studied and the effect of colchicine on SAA was demonstrated.
We conducted a retrospective cross-sectional study. Data were transferred from the hospital software and patients’ files of patients who were admitted to Istanbul University, Istanbul Medical Faculty, Department of General Pediatrics between January 2006, and December 2013, with recurrent fever, abdominal pain, and arthritis/arthralgia, and skin eruptions.
A total of 1064 patients were admitted to our clinic within this time period. Five hundred sixty-two children (52.8 %) were diagnosed as having FMF and comprised our study group. The age range of the study group was 1.8-16 years.
Tel-Hashomer diagnosis criteria 
1-Recurrent febrile episodes associated with peritonitis, pleuritis or synovitis
2-Amyloidosis of AA-type without a predisposing disease
3-Favorable response to daily colchicine
1-Recurrent febrile episodes
3-Positive history of familial Mediterranean fever in a first degree relative
Definite Diagnosis: The diagnosis if definite is 2 major or 1 major + 2 minor criteria are met.
Probable diagnosis: The diagnosis is probable if 1 major + 1 minor criterion are met.
Pras et al. severity scoring system for pediatric FMF 
Appearing of disease (year)
Frequency of attack on admission
Severity of arthritis
Required dosage of colchicine (mg/day)
The patients who had HSP underwent skin biopsy and immunoflorescence staining revealed deposition of IgA and C3 along small vessels.
The study was ethically approved by the ethics comitee within the Department of Pediatrics in our institution. Written and verbal consent was obtained from parents to use patient data for studies, but since this non-interventional study only reports our experience with patients managed according to the standard of care and patients did not undergo any tests that were requested solely for the purposes of obtaining data to include in this study, no separate consent for enrollment in the study was obtained.
SAA was measured in accordance with the manufacturer’s instructions (Siemens Health Care Diagnostic Products GmbH, Marburg/Germany) by N Latex SAA kits in Behring Nephelometer Prospec machine. C-reactive protein (CRP) was quantified with immunoturbidimetric methods as per the manufacturer’s instructions (Roche Diagnostics GmbH, Sandhoffer Strasse, Mannheim/Germany) by C-Reactive protein Latex kits (COBAS INTEGRA/Cobas System) in Roche Hitachi Cobas C 501 analyzer.
The assay for proteinuria was a quantitative one based on a 24 h urine collection. It was repeated one month after initiation of treatment with colchicine.
For 592 of the 1064 patients who reported fever, arthralgia and skin eruptions, autoinflammatory diseases were considered as a diagnostic possibility and therefore, analysis of the pertinent gene mutations were ordered. 562 of these cases turned out to have mutations.
Patients provided 2 cc blood under appropriate clinical conditions. DNA subtracts were taken from the blood samples using a QIAamp DNA mini kit (QIAGEN, catalog no: 51306). An FMF Strip Assay (ViennaLab Labordiagnostika GmbH, Vienna, Austria) kit was used to determine the presence of an Mediterranean fever (MEFV) gene mutation in patients. For mutation analysis, exon 2 v 10 of the MEFV gene was amplified using multiplex polymerase chain reaction (PCR) . Amplified products were hybridized with oligonucleotide probes. We screened for 12 MEFV gene mutations (E148Q in exon 2, P369S in exon 3, F479L in exon 5, M680I [G/C], M680I [G/A], 1692del, M694v, M6941, K695R, V726A, A744S, R761H in exon 10) using the FMF Strip Assay, Vienna Lab Diagnostics GmbH, Vienna, Austria. The mutations were called heterozygous, homozygous, and compound heterozygous.
Genetic mutation analysis was performed in Istanbul Medical Faculty Medical Biology laboratory. The white blood cell number, CRP, fibrinogen, erythrocyte sedimentation rate, SAA level, and protein amount in 24 h urine were investigated in the patients’ febrile periods. SAA level was also measured for a second time after treatment with colchicine in order to screen whether there was any influence with treatment.
Heterozygous patients were confirmed by sequence analyses.
Exon 2, 3, 5 and 10 was sequenced by using GML SeqFinder Sequencing System MEFV kit with Sanger sequence technology. The PCR conditions were as follows: Initial denaturation at 94 °C for 5 min, 35 cycles at 94 °C for 30 s and 58 °C for 45 s, 72 °C for 1 min, and a final extension at 72 °C for 5 min. The PCR products were visualized and collected with 2 % agarose gel electrophoresis, followed by purification using an Exo-SAP PCR purification Kit (UAB Corporation Cleveland, Ohio, USA). The product was sequenced in both strands initiating from the forward and the reverse primers used in the initial PCR and analysed on an ABI 3130 Automated DNA Sequencer (Applied Biosystems, Foster City, CA, USA). Further analysis was performed with SeqScape v2.6 and Sequencing Analysis 5.3.1 version programs .
All analyses were performed using SPSS 21.0. All continuous variables were examined using the paired or unpaired t-test as appropriate. Non-continuous variables were examined using the Chi-square test. The ratio of mutation types and clinical findings were compared with variance analysis. A P value < 0.05 for the two-tailed t-test was considered statistically significant.
Five hundred sixty-two children (52.8 %) were diagnosed as having FMF among the 1064 patients who presented with recurrent fever, abdominal pain, and arthritis/arthralgia and skin eruption (Fig. 1).
Patients and clinical findings
The past medical history, response to colchicine, symptoms and mutation types of patients with FMF on admission
Past Medical History
FMF in family history
Response to Colchicine
Type of Mutation
Results of mutation analysis
The heterozygote mutation was positive in 252 patients (44.8 %), homozygote mutations were positive in 228 patients (40.5 %), and compound heterozygote mutations were positive in 82 patients (14.6 %). The total positivity of mutations was as following: M694V (n = 290, 51.6 %), E148Q (n = 114, 20.2 %), M680I (n = 64, 11.3 %), R202Q (n = 57, 10.1 %), V726A (n = 18, 3.2 %), P369S (n = 9, 1.6 %), K695R (n = 7, 1.2 %) and U726A (n = 3, 0.5 %). The most frequently seen mutations with sequence analysis in heterozygote mutations were Met694Val (n = 129, 51.1 %), pVal726Ala (n = 92, 36.5 %) and pAla744Ser (n = 31, 12.4 %). The most frequently seen mutations in compound heterozygote patients were M694V/E148Q (n = 32 39 %).
The correlation of genetic mutations and symptoms
In total, 34 patients (6.04 %) were admitted with fever only, and their mean age was 2.1 ± 0.1 years. Of these patients, M694V was detected in 25 patients and R202Q homozygous mutation was found in 9 patients. The response to colchicine of all these patients was favorable.
Twenty-seven patients (4.8 %) who had no fever presented only with abdominal pain and their mean age was 4.5 ± 0.4 years. Among these patients, M694V was found in 20 patients and E148Q homozygote mutation was determined in 7 patients. The mean age of patients who were admitted with abdominal pain alone was significantly higher than those who presented only with fever (p = 0.04). Abdominal pain was significantly more frequent in patients with M694V and E148Q heterozygote mutation than in children with R202Q and M680I heterozygous mutations (p = 0.012).
The distribution of severity of FMF according to genetic mutations and types (n:562)
Homozygote mutations (n: 228; 40.5 %)
Heterozygote mutations (n: 252; 44.8 %)
Compound Heterozygote mutations (n: 82; 14.6 %)
The percentage of the clinically severe homozygote M694V mutations was 24.1 % (n = 70). This percentage was significantly higher than other homozygote mutations (p < 0.01).
Arthritis/arthralgia was significantly more common in patients with M694V and E148Q homozygous mutations (p = 0.014, p = 0.01, respectively).
Chest pain was more frequent in homozygous M694V (61,4 %) and heterozygous E148Q (25.6 %) mutation types (p = 0.04). Pericardial effusion was observed using echocardiography in 25 (10.9 %) of the 229 children with chest pain. The chest pain was unresponsive to colchicine in eight of these patients, consequently they were treated with methylprednisolone.
Skin eruptions were most commonly seen in homozygous E148Q mutations (p = 0.04). This was followed by heterozygous M694V and heterozygous M680I mutations.
The correlation of clinical findings and mutation types in patients with FMF (n:562)
Response to colchicine
M694V/ M680I (12/562)
The most common febrile episodes were in patients with M694V homozygous mutations (number of attacks = 4.4 ± 1.6/month). This was followed by compound heterozygous M694V-M680I mutations (number of attacks = 3.6 ± 1.1/month) and M680I-E148Q mutations (number of attacks = 2.3 ± 1.1/month).
Fever (n = 30), abdominal pain (n = 32), arthritis (n = 17) and arthralgia (n = 24) were the most common symptoms in compound heterozygous M694V-E148Q mutations.
The patients with compound heterozygous M694V/R202Q (n = 30, 36.5 %) mutations had skin eruptions (n = 16, 53.3 %) and HSP (n = 14, 36.6 %) in addition to fever and abdominal pain.
Patients with a history of appendectomy (n = 26) carried M694V homozygous mutations (n = 16) and E148Q homozygous mutation (n = 10).
Some of (n = 12, 2.29 %) the colchicine responsive patients (n = 524) had diarrhea after one week. We reduced the dose and continued the therapy.
There was no difference in the clinical features and genotypes of the cases required hospitalization and those that were managed as outpatients. The M694 mutation was prevalent in both groups.
Laboratory evaluations of patients with FMF
Mean ± SDS
8.58 ± 4.2
1 – 16
Leucocyte /mm 3
17.580 ± 5.571
5100 - 29700
64.5 ± 32.42
6 - 245
74.47 ± 32.24
8 - 132
463.24 ± 70.50
298 - 875
854 ± 145
520 - 2410
(positive in 106 patients)
Among the patients with proteinuria, homozygous M694V mutations were determined in 75 patients, homozygous M680I was in 12, homozygous E202Q was in 9, homozygous E148Q was in 6 patients, and other mutations were detected in 4 patients.
The response to colchicine therapy and serum level of SAA
The response to colchicine therapy
All of responsive
Before colchicine therapy
After colchicine therapy
Mean ± SD mg/dL
Mean ± SD mg/dL
234.2 ± 22.3
14.1 ± 1.4
154.3 ± 13.8
12.2 ± 1.3
182.1 ± 12.4
13.3 ± 1.2
Patients who had a partial response to monthly colchicine therapy (n = 38) had an average 156.34 ± 23.4 mg/dL SAA level. The level of SAA was significantly lower in complete responsive than in partial responsive (p = 0.001).
In this study we aimed to screen the correlation between genetic and phenotype of Turkish children who had been diagnosed as having FMF. Therefore, we investigated the 12 most frequent mutations and concomitant clinical and laboratory findings. The frequency of FMF among patients who were admitted with recurrent fever, abdominal pain, and arthritis/arthralgia and skin eruptions was 53.6 %. This result was similar to the study conducted by Ulgenalp et al. (50.5 %) .
The most common symptom was fever (97.3 %). The other frequent symptoms were abdominal pain (96.6 %) and arthritis/arthralgia (43.2 %/63.7 %). These clinical findings were mostly accompanied by M694V homozygous/heterozygous mutations. Similar to other studies, the most commonly seen mutation that accompanied clinical findings was M694V. Özelkaya et al. showed that the most frequent symptoms were abdominal pain (83.1 %) and fever (55 %). Other common findings reported are arthritis (17.1 %) and erysipelas-like erythema (7.7 %). It was also demonstrated that these clinical findings were mostly accompanied by M694V homozygote mutations [15–17].
Solak et al. reported the most common symptom to be abdominal pain, which was followed by fever, arthralgia, chest pain, and skin eruptions in a study of 165 patients. In this study, the most commonly seen mutations were M694V/I, E148Q and M680I . Akar et al. reported that the most frequent mutations were M694V and M680I . Giancane et al. reported that the E148Q variant is common, of unknown pathogenic significance and as the only MEFV variant does not support the diagnosis of FMF .
In our study, distinct from other studies, E148Q was the second most common mutation that accompanied fever, arthritis, and arthralgia. M680I was the third most common mutation and was found less frequently in patients with arthralgia/arthritis, but was seen more frquently in patients with skin eruptions.
Chest pain was most frequently seen in patients with M694V homozygous and E148Q heterozygous mutations. Similar to other studies, the M694V was the most commonly determined mutation in these patients.
Marek et al. researched the second other mutation apart from 12 mutations in patients with heterozygous MEFV gene mutations and demonstrated the second mutation in 25 % of patients . We did not investigate second analysis in patients with heterozygous mutations.
The mean age of patients who only had fever on admission was significantly lower than patients who presented with abdominal pain alone. It has been reported that fever is a common finding in younger patients; however, serositis, skin eruptions and other findings are more often seen in older patients with FMF . Padeh et al. also stated that the first symptom of the disease might be fever and serositis may develop later in the course . MEFV gene mutations can be found in patients with HSP. FMF has been reported more frequently in patients who had HSP than in the general population. MEFV mutations may be related to HSP susceptibility in children . Salah et al. found heterozygous mutations of V726A and E148Q to be the most common in children who also had HSP . In contrast, we found homozygous mutations of M694V and E148Q to be the most common. Dogan et al. found that 11 of their 76 patients (14.4 %) were heterozygous, and 5 patients (6.6 %) were homozygous and 2 were compound heterozygous . Altug et al., found that 18 of their 68 patients with HSP had MEFV mutations, 15 of them being heterozygous .
Our study included more patients who were first diagnosed with FMF and later went on to have HSP. This could be the reason why our study had more homozygous mutations in contrast to the findings of the three studies mentioned above .
In our study, in patients who had been previously diagnosed as having FMF and presented with findings pertinent to HSP, we found that the most common mutation of the 105 patients was M694V (n = 55, 52.3 %); the second most common was E148Q (n = 28, 26.6 %). Homozygous M694V and E148Q mutations were particularly common (p = 0.03).
FMF strip assay is a fast screening test; the most common major 12 mutations with known clinical meaning can be investigated. Screening can investigate only 12 mutations, whereas sequencing gives a result of all changes of exons 2,3,5 and 10 on MEFV gene that can be reviewed. More detailed sequencing tehcniques can reveal that clinically diagnosed patients who had none of the 12 most common mutations may actually have some of the less common mutations or novel mutations.
Proteinuria was reported to be positive most commonly with the M694V mutation and less frequent with E148Q .
Serum Amyloid A levels on admission with homozygous M694V mutation were significantly higher than with other mutations such as heterozygous and compound heterozygous mutations. Similar to the study of Berkun et al., the SAA level was higher in patients with homozygous M694V mutation . According to a study conducted by Duzova et al., SAA was higher with homozygous and compound heterozygous mutations . There was no significant difference in SAA level between mutation types in children with complete response. The level of SAA was significantly lower in patients who were completely responsive to colchicine than in partially responsive patients . Similar to our study, the authors emphasized that administration of colchicine might be effective in diminishing the SAA level . In our study, we showed a decrease in level of SAA in patients who had a complete response to colchicine therapy. The dose of colchicine was not increased.
A retrospective case series review was conducted of all MEFV gene mutation testing completed at UCLA Clinical Molecular Diagnostic Laboratory by Ong et al. to correlate specific genotypes with adverse phenotypes of affected populations residing in the Western United States, between February 2002, and February 2012. This was followed by a clinical chart review of all subjects who either had a single or double mutation. All 12 common mutations in the MEFV gene were analyzed and the M694V variant was found to be associated with an adverse FMF clinical outcome in the Armenian-American population, which manifested as earlier onset of disease, increased severity of disease, and renal amyloidosis .
In our study, M694V was found to be the most common mutation and it heralds more proteinuria and a more severe clinical course.
In summary, the frequency of FMF was 52.8 %. Fever was the most frequent symptom. The most common mutation was M694V. The mean age of patients who were admitted with abdominal pain alone was significantly higher than patients who presented with fever alone. Abdominal pain was significantly more frequent in patients with M694V and E148Q heterozygous mutations than children with R202Q and M680I heterozygous mutations. Arthritis/arthralgia were significantly more common in patients with homozygous M694V and E148Q mutations. Chest pain was more frequent with homozygous M694V (61.4 %) and heterozygous E148Q (25.6 %) mutations (p = 0.04). In 25 of the 229 children (10.9 %) with chest pain, pericardial effusion was documented at echocardiography. Skin eruption was most commonly seen in homozygous E148Q mutations. This was followed by heterozygous M694V and heterozygous M680I mutations. Homozygous M694V (n = 34, 32.3 %) and E148Q (n = 23, 22 %) mutations were significantly more frequent in patients with HSP (p = 0.03). Arthritis (n = 17, 7.0 %) and arthralgia (n = 24, 6.7 %) were seen more frequently in patients with compound heterozygous M694V/E148Q mutations, whereas M694V/R202Q coexistence caused skin eruptions (n = 16, 11.4 %) more frequently. The most frequent occurence of febrile episodes were in patients with M694V homozygous mutations (number of attacks = 4.4 ± 1.6/month). Patients with a history of appendectomy (n = 26) carried homozygous M694V (n = 16) and E148Q (n = 10) mutations. Diarrhea developed after colchicine therapy in 0.22 % of patients. The ratio of the clinically-severe patients was 24.1 % (n = 70) in children with homozygous M694V mutations. This ratio was significantly higher than other homozygous mutations. Proteinuria was detected most frequently in patients with homozygous M694V mutations. The SAA level in homozygous M694V mutations was significantly higher than in other mutations.
Our study was comprehensive and has demonstrated the correlation between the genotype and the clinical characteristics of FMF in Turkish children. Patients were classified and analyzed according to clinical, laboratory, and genotype features. However, a major limitation of our study is its retrospective design and the lack of a demographic analysis due to insufficient information about the place of birth of the patients.
David Chapman contributed to the manuscript by correcting the grammar.
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- Onen F. Familial Mediterranean fever. Rheumatol Int. 2006;26:489–96.PubMedView ArticleGoogle Scholar
- Hesker PR, Nguyen M, Kovarova M, Ting JP, Koller BH. Genetic loss of murine pyrin, the Familial Mediterranean Fever protein, increases interleukin-1β levels. PLoS One. 2012;7:e51105.PubMedPubMed CentralView ArticleGoogle Scholar
- Kisacik B, Yildirim B, Tasliyurt T, Ozyurt H, Ozyurt B, Yuce S, et al. Increased frequency of familial Mediterranean fever in northern Turkey: a population-based study. Rheumatol Int. 2009;29:1307–9.PubMedView ArticleGoogle Scholar
- Etem E, Derya DS, Erol D, Yuce H, Elyas H. Familial Mediterranean fever: a retrospective clinical and molecular study in the East of Anatolia region of Turkey. Open Rheumatol J. 2010;4:1–6.PubMedPubMed CentralView ArticleGoogle Scholar
- Kosan C, Cayir A, Turan MI. Relationship between genetic mutation variations and acute-phase reactants in the attack-free period of children diagnosed with familial Mediterranean fever. Braz J Med Biol Res. 2013;46:904–8.PubMedPubMed CentralView ArticleGoogle Scholar
- Kucuk A, Gezer IA, Ucar R, Karahan AY. Familial Mediterranean Fever. Acta Medica (Hradec Kralove). 2014;57(3):97–104.View ArticleGoogle Scholar
- French FMF Consortium. A candidate gene for familial Mediterranean fever. Nat Genet. 1997;17(1):25–31.View ArticleGoogle Scholar
- Dundar M, Kiraz A, Emirogullari EF, Saatci CE, Taheri S, Baskol M, et al. A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients. Ann Saudi Med. 2012;32:343–8.PubMedView ArticleGoogle Scholar
- Papadopoulos VP, Giaglis S, Mitroulis I, Ritis K. The population genetics of familial mediterranean fever: a meta-analysis study. Ann Hum Genet. 2008;72:752–61.PubMedView ArticleGoogle Scholar
- Samli H, Dogru O, Bukulmez A, Yuksel E, Ovali F, Solak M. Relationship of Tel Hashomer criteria and Mediterranean fever gene mutations in a cohort of Turkish familial Mediterranean fever patients. Saudi Med J. 2006;27:1822–6.PubMedGoogle Scholar
- Pras E, Livneh A, Balow Jr JE, Pras E, Kastner DL, Pras M, et al. Clinical differences between North African and Iraqi Jews with familial Mediterranean fever. Am J Med Genet. 1998;75:216–9.PubMedView ArticleGoogle Scholar
- Tchemitchko D, Legendre M, Delahaye A, Cazeneuve C, Niel F, Goossens M, et al. Clinical evaluation of a reverse hybridization assay for the molecular detection of twelve MEFV gene mutations. Clin Chem. 2003;49:1942–5.View ArticleGoogle Scholar
- Dogan H, Akdemir F, Tasdemir S, Atis O, Diyarbakir E, Yildirim R, et al. A novel insertion mutation identified in exon 10 of the MEFV gene associated with Familial Mediterranean Fever. BMC Med Genet. 2014;15:74.PubMedPubMed CentralView ArticleGoogle Scholar
- Ulgenalp A. The distribution of MEFV Gene mutations in the referrals to DEQETAM. DEÜ Tıp Fakültesi Dergisi. 2009;23:53–8.Google Scholar
- Ozalkaya E, Mir S, Sozeri B, Berdeli A, Mutlubas F, Cura A. Familial Mediterranean fever gene mutation frequencies and genotype-phenotype correlations in the Aegean region of Turkey. Rheumatol Int. 2011;31:779–84.PubMedView ArticleGoogle Scholar
- Yigit S, Bagci H, Ozkaya O, Ozdamar K, Cengiz K, Akpolat T. MEFV mutations in patients with familial Mediterranean fever in the Black Sea region of Turkey: Samsun experience. J Rheumatol. 2008;35:106–13.PubMedGoogle Scholar
- Olgun A, Akman S, Kurt I, Tuzun A, Kutluay T. MEFV mutations in familial Mediterranean fever: association of M694V homozygosity with arthritis. Rheumatol Int. 2005;25:255–9.PubMedView ArticleGoogle Scholar
- Solak M, Yildiz H, Koken R, Erdogan MO, Eser B, Sen TA, et al. Analysis of MEFV Gene mutations in 165 patients formerly diagnosed as familial Mediterranean fever. Turkiye Klinikleri J Med Sci. 2008;28:117–22.Google Scholar
- Akar N, Misirlioglu M, Yalcinkaya F, Akar E, Cakar N, Tumer N, et al. MEFV mutations in Turkish patients suffering from familial Mediterranean fever. Hum Mutat. 2000;15:118–9.PubMedView ArticleGoogle Scholar
- Giancane G, Ter Haar NM, Wulffraat N, Vastert SJ, Barron K, Hentgen V, et al. Evidence-based recommendations for genetic diagnosis of familial Mediterranean fever. Ann Rheum Dis. 2015;74(4):635–41.PubMedView ArticleGoogle Scholar
- Marek-Yagel D, Berkun Y, Padeh S, Abu A, Reznik-Wolf H, Livneh A, et al. Clinical disease among patients heterozygous for familial Mediterranean fever. Arthritis Rheum. 2009;60:1862–6.PubMedView ArticleGoogle Scholar
- Padeh S, Livneh A, Pras E, Shinar Y, Lidar M, Feld O, et al. Familial Mediterranean Fever in the first two years of life: a unique phenotype of disease in evolution. J Pediatr. 2010;156:985–9.PubMedView ArticleGoogle Scholar
- Padeh S, Livneh A, Pras E, Shinar Y, Lidar M, Feld O, et al. Familial Mediterranean fever in children presenting with attacks of fever alone. J Rheumatol. 2010;37:865–9.PubMedView ArticleGoogle Scholar
- Salah S, Rizk S, Lotfy HM, El Houchi S, Marzouk H, Farag Y. MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura. Pediatr Rheumatol Online J. 2014;12:41.PubMedPubMed CentralView ArticleGoogle Scholar
- Ozcakar ZB, Elhan AH, Yalcinkaya F. Can colchicine response be predicted in familial Mediterranean fever patients? Rheumatology (Oxford). 2014;53:1767–72.View ArticleGoogle Scholar
- Dogan CS, Akman S, Koyun M, Bilgen T, Comak E, Gokceoglu AU. Prevalence and significance of the MEFV gene mutations in childhood Henoch-Schönlein purpura without FMF symptoms. Rheumatol Int. 2013;33:377–80.PubMedView ArticleGoogle Scholar
- Altug U, Ensari C, Sayin DB, Ensari A. MEFV gene mutations in Henoch-Schönlein purpura. Int J Rheum Dis. 2013;16:347–51.PubMedView ArticleGoogle Scholar
- Topaloglu R, Ozaltin F, Yilmaz E, Ozen S, Balci B, Besbas N, et al. E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever. Ann Rheum Dis. 2005;64:750–2.PubMedPubMed CentralView ArticleGoogle Scholar
- Berkun Y, Padeh S, Reichman B, Zaks N, Rabinovich E, Lidar M, et al. A single testing of serum amyloid a levels as a tool for diagnosis and treatment dilemmas in familial Mediterranean fever. Semin Arthritis Rheum. 2007;37:182–8.PubMedView ArticleGoogle Scholar
- Duzova A, Bakkaloglu A, Besbas N, Topaloglu R, Ozen S, Ozaltin F, et al. Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever. Clin Exp Rheumatol. 2003;21:509–14.PubMedGoogle Scholar
- Hentgen V, Grateau G, Kone-Paut I, Livneh A, Padeh S, Rozenbaum M, et al. Evidence-based recommendations for the practical management of Familial Mediterranean Fever. Semin Arthritis Rheum. 2013;43:387–91.PubMedView ArticleGoogle Scholar
- Ong FS, Vakil H, Xue Y, Kuo JZ, Shah KH, Lee RB, et al. The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA. Clin Genet. 2013;84:55–9.PubMedPubMed CentralView ArticleGoogle Scholar