肌病性萎縮 的英文怎麼說

中文拼音 [bìngxìngwēisuō]
肌病性萎縮 英文
myopathic atrophy
  • : 名詞1. (肌肉) muscle; flesh 2. [書面語] (皮膚) skin
  • : Ⅰ名詞1 (疾病; 失去健康的狀態) illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • : Ⅰ名詞1 (性格) nature; character; disposition 2 (性能; 性質) property; quality 3 (性別) sex ...
  • : 萎動詞(衰落) decline; wane
  • : 縮構詞成分。
  • 萎縮 : 1 (乾枯) wither; shrivel 2 (經濟衰退) shrink; sag; contraction3 [醫學] depauperate; analosis;...
  1. A gene implicated in spinal muscular atrophy showed an association in three populations, but not in yoruba from ibadan, nigeria

    一個涉及脊髓的基因顯示出與三個人群有關聯但卻沒有在伊巴丹、奈及利亞、的優魯巴人身上發現。
  2. The illnesses that challenge these children range from cancer, cystic fibrosis and leukemia to cerebral palsy, muscular dystrophy, and aids

    那些小孩的疾包括癌癥腦麻痹血癌脊椎癱瘓癥及愛滋
  3. “ i have two sons. my older son is 22 and is in an advanced stage of muscular dystrophy. my younger son is 21 and has been diagnosed as chronically mentally ill

    我有2個兒子.我的大兒子22歲,已經是癥的晚期.我的小兒子21歲,被診斷為慢精神疾
  4. There is loss of anterior horn cells, so that patients present with progressive weakness that proceeds to paralysis from neurogenic muscular atrophy

    存在前角細胞喪失,因此人表現為漸進衰弱,這可能因神經源而出現癱瘓。
  5. Alternatively, they could generate healthy specialized cells from patients who had donated their genetic material, and transplant them into tissues - - without the risk of prompting immune rejection - - to treat failing hearts, neurological diseases such as parkinson ' s disease and amyotrophic lateral sclerosis, spinal cord injury and diabetes

    上述二者中,他們可從被診為患遺傳疾人中生成指定的健康細胞,並將其移植培養為組織不存在排斥免疫方面的風險可治療心臟衰竭,神經疾如帕金森癥,(脊髓)側索硬化癥,骨髓癥和糖尿
  6. Pathological changes of amyotrophic lateral sclerosis with in vivo magnetic resonance spectrum and diffusion tensor imagings

    在體磁共振波譜及擴散張力成像觀察側索硬化的理變化的研究
  7. Results the clinical features showed progressive muscle weakness in upper limb ; emg showed neurogenic changes, motor and sensory nerve conductive velocity was normal ; nerve repetetive stimulation showed decreased response ; muscle histochemistry revealed neurogenic findings ; ultra - eletronmicroscopy was not abnormal

    結果該例患者表現為進行肉力弱,電圖顯示神經源損害,神經重復刺激檢查示波幅下降,理顯示小簇狀,電鏡下除極少數纖維膜溶解外其他未見特殊。
  8. Inherited gene mutations, such as those that cause hemophilia or muscular dystrophy, would have to be corrected as well before using a patient ' s own cells to create es cells

    在使用帶有遺傳基因突變(例如血友肉營養癥)患者的細胞來製造胚胎幹細胞之前,也需要先矯正缺陷基因。
  9. The patient was a 71 year old man who developed muscle wasting and weakness and had electromyographic evidence of motor neuron disease

    患者是71歲男,漸發和無力,電圖描記的證據顯示為運動神經元
  10. Heriditary neuropathies come in many shapes and sizes. charcot - marie - tooth type 2 ( cmt2 ) causes degeneration of peripheral sensory and motor neurons, particularly at the ends of these long axons

    遺傳神經具有多種特點和方式。 2型腓骨癥( cmt 2 )導致外周特別是長軸突末端的感覺和運動神經元退化。
  11. The underlying pathogenesis of steroid - induced myopathy associated with chronic use is a non - necrotic atrophic myopathy resulting in proximal muscle weakness without muscle pain or tenderness

    用藥導致的類固醇誘導是一種非壞死,導致近端無力不伴有肉疼痛和壓痛。
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