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short status
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  “short status”译为未确定词的双语例句
     Physical examination of the only survival patient showed short status (165 cm) , arched feet and poor reaction of the left side nose-pointed test.
     1例存活者,临床检查:身材矮小,弓形足,左侧轮替指鼻试验反应差;
短句来源
     Clinical features include microspherophakia, lens ectopia, glaucoma, brachydactyly, short status and so on.
     临床表现为球形晶状体、晶状体脱位、青光眼、短指、身材矮小等。
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  相似匹配句对
     The Status and Development of Short Stories in French Literature
     短篇小说在法国文学史中的地位与发展
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     This status can be explained by the short of research.
     这种状况与近年来研究方法等方面的缺失密切相关。
短句来源
     Status in Beijing
     北京的城市雕塑
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     On the Status of Rhetoric
     修辞学是否属于言语语言学的大讨论
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     gubernaculum short.
     引带短。
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  short status
In this contribution we give a short status report of the project underlining the highlights achieved so far.
      
We present a short status report of activities that have taken place to deal with some of the technical and scientific issues that were discussed.
      
In this contribution we give a short status report of the project underlining the highlights achieved so far.
      


Four sibling of a family with Alper' s disease were reported. Three of them occurred diarrhea and myoclonus at the ages of 6 to 8 years old. During the disease development, symptoms of subacute en-cephalopathy such as headache, visual disturbance, cortical blindness, progressive seizures and mental retardation were presented at the ages of 16 to 20 years old. The downhill progression of disease resulted in death within six to eight months of onset. CT showed hypodensity lesions in the bilateral occipital and...

Four sibling of a family with Alper' s disease were reported. Three of them occurred diarrhea and myoclonus at the ages of 6 to 8 years old. During the disease development, symptoms of subacute en-cephalopathy such as headache, visual disturbance, cortical blindness, progressive seizures and mental retardation were presented at the ages of 16 to 20 years old. The downhill progression of disease resulted in death within six to eight months of onset. CT showed hypodensity lesions in the bilateral occipital and temporal lobes. Spongiform changes, which characterized by diffuse neuronal degeneration or loss and astrocytosis, were found most severe in the gray matter. White matter was slightly involved, but basal ganglia, pons, brain stem and cerebellum were not involved. Physical examination of the only survival patient showed short status (165 cm) , arched feet and poor reaction of the left side nose-pointed test. Muscle biopsy of him showed a large amount of Red-Ragged (RR) fibers and abnormal mitochondria. Clinical features and pathological findings of autopsy in all the four patients were consistent with progressive neuronal degeneration of childhood (PNDC) - Alper' s disease. The muscle biopsy showed the characteristic findings of mitochondrial encephalomyopathy. It is considered that the late onset Alper's disease may be classified as a type of mitochondrial encephalomyopathy.

一家系4兄妹,3人均在6~8岁发生腹泻、抽搐。16~20岁出现亚急性头痛、失明、皮层盲、抽搐发作、智能衰退,进行性加重6~8个月因衰竭而死亡。头颅CT扫描显示,双侧枕、颞叶低密度病变;大脑病理学特点为全脑灰质层状神经细胞变性脱失、星形细胞增生,呈海绵状脑灰质萎缩,但白质受累较轻,不累及基底节、丘脑、脑干和小脑。1例存活者,临床检查:身材矮小,弓形足,左侧轮替指鼻试验反应差;肌肉活组织检查可见大量不整红边纤维和异常线粒体。根据临床神经病理学特点该病症属于进行性脑灰质萎缩Alper病;而肌肉病理学特征则归于线粒体脑肌病。推测晚发型Alper病可能是线粒体脑肌病的一种类型。

Machesani syndrome is characterized of brachydactyly and microspherophakia. Clinical features include microspherophakia, lens ectopia, glaucoma, brachydactyly, short status and so on. One case of Marchesani syndrome was reported and relative literatures were reviewed. The mechanism, clinical features, points in diagnosis and treatment on this disease are discussed in this paper.

Marchesani综合征是一种以短指和球形晶状体为主要特征的综合征。临床表现为球形晶状体、晶状体脱位、青光眼、短指、身材矮小等。本文报告1例并结合复习文献,对本病的发病机制、临床特征及诊断治疗要点作一介绍。

 
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