頁籤選單縮合
題 名 | Fetal Warfarin Syndrome=胎兒Warfarin症候群 |
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作 者 | 侯家瑋; | 書刊名 | 長庚醫學 |
卷 期 | 27:9 2004.09[民93.09] |
頁 次 | 頁691-695 |
分類號 | 417.107 |
關鍵詞 | 胎兒warfarin症候群; 抗凝血劑; 胚胎病; Fetal warfarin syndrome; Anticoagulant; Embryopathy; |
語 文 | 英文(English) |
中文摘要 | 胎兒warfarin症候群是一種極罕見的胚胎病,主要是因為胎兒長期暴露於使用warfarin之母體後受到傷害所致。一名男孩因母親罹患風濕性心臟病接受機械性心臟瓣膜置換後,需要服用抗凝血劑warfarin而罹患胎兒warfarin症候群,特徵包括鼻樑低下、喉頭軟化、雞胸、先天性心臟病、腦室擴大、點狀性軟骨形成不良、手指畸形及生長遲滯。本文將討論胎兒warfarin症候群其致病機及處理方式。 |
英文摘要 | Fetal warfarin syndrome (FWS) or warfarin (coumadin) embryopathy is a rare condition as a result of fetal exposure to maternal ingestion of warfarin during pregnancy. A male infant, whose mother was treated with the anticoagulant (warfarin) because of a mechanical heart valve replacement after rheumatic heart disease, presented with signs of warfarin embryopathy. The facial dysmorphism included hypoplasia of nasal bridge, laryngomalacia, pectus carinatum, congenital heart defects (atrial septal defect and patent ductus arteriosus), ventriculomegaly, stippled epiphyses, telebrachydactyly, and growth retardation. The apthogenesis and management of FWS are discussed. |
本系統中英文摘要資訊取自各篇刊載內容。