Turk, SenaAydin, DeryaDogan, EserLevent, ErturkKutukculer, Necil2020-12-012020-12-0120201047-95111467-1107https://doi.org/10.1017/S1047951120001444https://hdl.handle.net/11454/62182Kawasaki disease, known as mucocutaneous lymph node syndrome, is a multi-system disease of unknown aetiology that occurs in young children under 5 years of age. the recurrence rate of Kawasaki disease is as rare as 1-3%. Especially in cases with coronary artery involvement, recurrent Kawasaki disease should be investigated in terms of underlying rheumatologic diseases such as periodic fever syndromes, microscopic polyangiitis, polyarteritis nodosa, and systemic-onset juvenile arthritis. in this study, we report homozygote mutations in mevalonate kinase and familial Mediterranean fever genes in a recurrent Kawasaki disease with coronary dilatation.en10.1017/S1047951120001444info:eu-repo/semantics/closedAccessFamilial Mediterranean feverhyperimmunoglobulin D syndromeKawasaki diseaseperiodic fever syndromesArticle30710091011WOS:0005624700000162-s2.0-8508703963432524933Q3Q4