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頁籤選單縮合
題名 | 脊髓性肌肉萎縮症=Spinal Muscular Atrophy |
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作者 | 周莉莉; 王如華; 陳錫洲; Chou, Lih-lih; Wang, Ru-hwa; Chen, Shyi-jou; |
期刊 | 國防醫學 |
出版日期 | 20001200 |
卷期 | 31:6 2000.12[民89.12] |
頁次 | 頁759-764 |
分類號 | 415.9413 |
語文 | chi |
關鍵詞 | 脊髓性肌肉萎縮症; 運動神經元; 遺傳; Spinal muscular atrophy; Motor neuron; Inheriance; |
中文摘要 | 脊髓性肌肉萎縮症是一群因運動神經元退化而造成肌肉萎縮、無力的遣傳性疾病。國內每年約有三十至四十位罹患此症之嬰兒出生,一旦罹患此症,隨即會對家庭造成相當大的衝擊。 本篇文章之主要目的在對脊隨性肌肉萎縮症之臨床病理、分類、症狀、診斷及治療等加以描述,期望醫護同仁及社會大眾對此症有更深一層之認識及瞭解。進而提供脊髓性肌肉萎縮症患者及家庭適當之護理與相關的諮詢服務。 |
英文摘要 | Spinal muscular atrophy (SMA) is the name given to a group of inherited disease characterized by muscle weakness and wasting cause of motor neurons defect. The incidence is nearly thirty to forty live births baby are affected in each year. When the diagnosis was established, it inevitably has a tremendous impact on the entire family. The purpose of this article was to describe the clinical pathology, classification, symptoms, diagnosis, and the treatment of spinal muscular atrophy. To expect the physicians, nurses and clients are concerned for spinal muscular atrophy, and to provide nursing and counseling services of the clients and families. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。