Identify Han Chinese Population-Specific Genetic Mutations in Patients with Tetralogy of Fallot and Develop a Genetic Risk Prediction Model for Clinical Practice (I)

2023-08-012025-04-21https://scholars.lib.ntu.edu.tw/handle/123456789/728421華人法洛氏四重症臨床資料及特有的基因突變資料仍少，建構心律不整,右心衰竭的早期風險評估工具,是臨床重要的參考。建構危險預測模式，將可預測病人未來心律不整發作，心衰竭的風險，提早藥物劑量或種類調整，降低再發作機會，另外可協助國家制定法洛氏四重症病童的最佳治療策略.法洛氏四重症華人法洛氏四重症特有突變基因基因風險評分Tetralogy of Fallotpopulation-specific TOF mutationsgenetic risk scoresIdentify Han Chinese Population-Specific Genetic Mutations in Patients with Tetralogy of Fallot and Develop a Genetic Risk Prediction Model for Clinical Practice (I)