查詢結果分析
相關文獻
- Central Core Disease with Family History of Malignant Hyperthermia: Report of One Case
- 桿狀體肌肉病變
- Elimination of Hypercapnia May Postpone the Clinical Presentation of Malignant Hyperthermia: A Case Report
- 甲狀腺低下症肌肉病變:一病例報告
- HMG CoA還原酶抑制劑背後的陰影--肌肉病變
- Hypothyroid Myopathy-Pathological and Ultrastructural Study
- 非侵襲性呼吸器--神經肌肉病變患者之另一種選擇
- Congential Myopathy with Uniform Type 1 Fiber Predominance and Type 2 Fiber Hypoplasia:Report of One Case
- Early Recognition of Unsuspected Malignant Hyperthermia and Successful Management of Severe Myoglobinuric Renal Failure in Subsequent Rhabdomyolysis: A Case Report
- 發炎性肌肉病變
頁籤選單縮合
題名 | Central Core Disease with Family History of Malignant Hyperthermia: Report of One Case=中心蕊疾病合併惡性高溫之家族史:一病例報告 |
---|---|
作者 | 李英齊; 陳永榮; 方鵬程; Lee, Inn-chi; Chen, Yung-jung; Fang, Peng-cheng; |
期刊 | 臺灣兒科醫學會雜誌 |
出版日期 | 20070700、20070800 |
卷期 | 48:4 2007.07-08[民96.07-08] |
頁次 | 頁217-219+240 |
分類號 | 415.9413 |
語文 | eng |
關鍵詞 | 中心蕊疾病; 惡性高溫; 肌肉病變; Central core disease; Malignant hyperthermia; Myopathy; |
中文摘要 | 兒童中心蕊疾病合併家族性惡性高溫為一罕見的疾病。在此報告一病例在10個月大嬰兒有動作發展遲緩與下肢肌肉無力。其祖母死於開刀時惡性高溫。在五歲時神經學檢查發現,近端肌肉輕微無力且萎縮,深部肌腱反射降低但智力正常,肌電圖顯示為肌肉病變。肌肉切片顯示第一型肌肉纖維萎縮且有中心蕊構造。 |
英文摘要 | A 10-month-old boy presented with gross motor delay and muscle weakness, especially in both lower limbs. At age 5, he developed lordosis, talipes, and planovalgus. His grandmother died of malignant hyperthermia during surgery. On neurological examination, he had mild proximal muscle weakness and atrophy, decreased deep tendon reflexes and Gowers' sign, but his intelligence was normal. The electromyogram showed myopathic pattern. Muscle biopsy revealed type 1 fiber atrophy and central core abnormalities. We report this case of central core disease with a family history of malignant hyperthermia during surgery. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。