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                                                                                                                                                                                                                             analysis included only the three most frequent mutations in
                                                                                                                                                                                                                             ber of patients. In addition, like most previous studies, our
                                                                                                                                                                                                                           The limitations of the present study include the small num-
                                                                                                                                                                                                                             may be offerred to populations at high risk.
                                                                                                                                                                                                                             guinity rate in the population. In addition, genetic counseling
                                                                                                                                                                                                                             high among the population), and minimization of the consan-
                                                                                                                                                                                                                             dietary changes, reduction in the rate of smoking (which is very
                                                                                                              KEY WORDS:
                                                                                                                                                                                                                             Preventive intervention that has been suggested includes
                                                                                                                                                                                                                             ties are very important and could have an important impact.
                                                                                                                                                                                                                             incidence and prevalence in the future. Also, educational activi-
                                                                                                                                                                                                                             tors had led us to expect a continuation of the increase in IBD
                                                                                                                                                                                                                             19 years [1]. The compensation of these aforementioned fac-
                                                                                                                                                                                                                             young society, with 60% of the population younger than age
                                                                                                                                                                                                                           The Bedouin Arab population in southern Israel is a very
                                                                                                                                                                                                                             of the NOD2/CARD15 mutation in this specific population.
                                                                                                                                                                                                                             nutrition. However, as we expected, we found a high prevalence
                                                                                                                                                                                                                             with a Western lifestyle, particularly with regard to hygiene and
                                                                                                                                                                                                                             change of lifestyle, including urbanization and modernization
                                                                                                                                                                                                                             Bedouin Arab is increasing [2], which may be attributed to the
                                                                                                                                                                                                                           We have reported before that the incidence of IBD among
                                                                                                                                                                                                                             clinical characteristics of the UC patients.
                                                                                                                                                                                                                             sis, no other differences were found regarding demographic or
                                                                                                                                                                                                                             P = 0.06) in the UC cohort. In our genotype-phenotype analy-
                                                                                                                                                                                                                             cally non-significant (46.7 ± 16.1 years vs. 30.7 ± 12.7 years;
                                                                                                                                                                                                                             higher among mutation carriers by about 15 years, but statisti-
                                                                                                                                                                                                                           In a genotype-phenotype analysis, age at diagnosis was
                                                                                                                                                                                                                             reported frequency in different ethnic groups [12-14].
                                                                                                                                                                                                                             is a relatively high-frequency rate compared with previously
                                                                                                                                                                                                                             the NOD2/CARD15 mutation in three patients (12%), which
                                                                                                                                                                                                                           The present study included 25 patients with UC. We found
                                                                                                                                                                                                                             including disease location and behavior.
                                                                                                                                                                                                                           In our study, no association was found in other parameters,
                                                                                                                                                                                                                             previously [6-9].
                                                                                                                                                                                                                             carrier group (P = 0.005). This finding has not been reported
                                                                                                                                                                                                                             mutation carriers were male, compared to 41% in the non-
                                                                                                                                                                                                                             tionship. Our results showed that 100% of the NOD2/CARD15
                                                                                                                                                                                                                             An important finding of the present work is the gender rela-
                                                                                                                                                                                                                             Similar findings were reported in previous studies [8,9,16,18].
                                                                                                                                                                                                                                                        131118-COHANIM - 131118-COHANIM | 4 - A | 18-11-13 | 11:24:13 | SR:-- | Cyan
                                                                                                                                                                                                                             riers compared to 28.82 ± 9.1 years in non-carriers (P = 0.04).
                                                                                                                                                                                                                                                        #131118-COHANIM - 131118-COHANIM | 4 - A | 18-11-13 | 11:24:13 | SR:-- | Black
                                                                                                                                                                                                                                                        131118-COHANIM - 131118-COHANIM | 4 - A | 18-11-13 | 11:24:13 | SR:-- | Yellow
                                                                                                              ABSTRACT:
                                                                                                                                                                                                                             age on onset, with the age of 22.8 ± 4.5 years in mutation car-
                                                                                                                                                                                                                                                        131118-COHANIM - 131118-COHANIM | 4 - A | 18-11-13 | 11:24:13 | SR:-- | Magenta
                                                                                                                                                                                                                             relationship between the NOD2/CARD15 mutation and early
                                                                                                                                                                                                                             [5-10]. Our results, in agreement with other studies, showed a
                                                                                                                                                                                                                             genotype correlations of NOD2/CARD15 in CD patients
                                                                                                                                                                                                                           There is a large number of reports regarding phenotype-
                                                                                                                                                                                                                             genetic investigation in the future.
                                                                                                                                                                                                                             population could be an interesting population for further
                                                                                                                                                                                                                             nuclear families; each includes four patients with IBD. This
                    3,4
                                                                                                                                                                                                                           In the current IBD Bedouin Arab cohort, there are two
                                                                                                                                                                                                                             explain the high prevalence of genetic disease [4].
                                                                                                                                                                                                                             to have a high rate of consanguinity marriage, which might
                                                                                                                                                                                                                             and no more than 13%. The Bedouin Arab population is known
                                                                                                                                                                                                                             of Israel, which showed a lower frequency of mutation carriage
                                                                                                                                                                                                                                                        #
       Original articles    Original articles  3,4   and   Micha J. Rapoport MD  edication non-adherence may reduce the effectiveness   1 October 2013 and 31 March 2014 were retrieved from the   Center with recommendation for BB insulin regimen between   from the internal medicine wards of Assaf Harofeh Medical   Demographic and clinical data of T2DM patients discharged   DATA RETRIEVAl  This research was a retrospective single center study.  PATIENTS AND METHODS  recomme
                   earlier, known risk factors for such recurrences include previ-  Correspondence                               17.  Fidder H, Olschwang S, Avidan B, et al. Association between mutations in the   22.  Abreu  MT, Taylor  KD,  Lin  YC,  et  al.  Mutations  in  NOD2  are associated  with
                   ous anastomotic leak and congenital esophageal stenosis. No   Dr. l. Bentur                                     CARD15(NOD2) gene and Crohn’s disease in Israeli Jewish patients. Am J Med   fibrostenosing disease in patients with Crohn’s disease. Gastroenterology 2002; 123:
                                                                                                                                   Genet 2003; 121A: 240-4.
                   differences in short-term complication rates, anastomotic leak,   Director, Dept. of Pediatric Pulmonology, Rappaport Children’s Hospital,   18.  Zouiten-Mekki L, Zaouail H, Boubaker Jet al. CARD15/NOD2 in a Tunisian   679-88.
                   or anastomotic stricture were found between the thoracoscopic   Rambam Health Care Campus, Haifa 3109601, Israel  population with Crohn’s disease. Dig. Dis. Sci 2005; 50 (1): 130-5.  23.  Bhullar M, Macrae F, Brown G, et al. Prediction of Crohn’s disease aggression
                                                                   phone: (972-4) 777-4360, fax: (972-4) 777-4395
                   and open approaches [14].                       email: l_bentur@rambam.health.gov.il                          19.   Hama I, Ratbi I, Reggoug S, et al. Non-association of Crohn’s disease with NOD2   through NOD2 /CARD15 gene sequencing in an Australian cohort.  World  J
                                                                                                                                                                                   Gastroenterol 2014; 20 (17): 5008-16.
                     In the current evaluation, the only factors associated with   References                                      gene variants in Moroccan patients. Gene 2012; 499: 121-3.
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                   of TEF were immunologically intact. We postulate that, fol-  8.  Shah R, Varjavandi V, Krishnan U. Predictive factors for complications in children   colleagues performed intervention studies in which smooth   that IL-1β has multiple beneficial effects in late-stage murine
                   lowing TEF repair, the tracheoesophageal area might be more   with esophageal atresia and tracheoesophageal fistula. Dis Esophagus 2015; 28 (3):   muscle cell (SMC) lineage-tracing Apoe-/- mice with advanced   atherosclerosis, including promotion of outward remodeling
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