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A Comparison of the Ghent and Revised Ghent Nosologies for the Diagnosis of Marfan Syndrome in an Adult Korean Population
성균관의대 삼성서울병원
양정훈, 한혜진, 장신이, 문주령, 성기익, 정태영, 이흥재, 기창석, 김덕경
Background: Recently, a revised Ghent nosology has been established for the diagnosis of Marfan syndrome (MFS) that puts more weight on the aortic root aneurysm and ectopia lentis. We compared the application of the Ghent and revised Ghent nosologies in adult Korean patients for whom there is suspicion of MFS. Methods: From January 1995 to June 2010, we enrolled 106 patients older than 20 years for whom there was suspicion of MFS, and who had undergone genetic analysis of the fibrillin-1 gene (FBN1). Results: Of 106 patients, 86 patients (81%) fulfilled the criteria of the Ghent nosology, and 84 patients (79%) met the criteria of the revised Ghent nosology. The two patients who met the Ghent nosology criteria, but not the criteria of the revised Ghent nosology were diagnosed with Loeys-Dietz syndrome and MASS phenotype. The level of agreement between both nosologies was very high (κ=0.94, 95% confidence interval: 0.86 to 1.0). Marfan-like syndromes were diagnosed in 30% (6/20 patients) with negative Ghent and revised Ghent criteria and no FBN1 mutations. Conclusions: These results suggest that the revised Ghent nosology is not inferior to the Ghent nosology for the diagnosis of MFS in adult Korean patients.


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