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Neurologic symptoms of hypermagnesemia are muscular weakness, paralysis, ataxia, drowsiness, and confusion.

高镁血症的神经系统症状表现为肌肉无力、瘫痪、、嗜睡和意识模糊。

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Babinski signs were negative.Gait was slow, broadbased, and tandem walking was ataxic.

态沉重,缓慢,似鸭

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Symptoms such as nausea,vomiting,dizziness and dystaxia were common in this group of patients,and headache and nuchal rigidity were found in 51.6% and 32.3% patients respectively.

人以恶心呕吐、眩晕和为常见临床表现,而头痛和颈项强直仅分别见于51.6%和32.3%的人。

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NS syndrome:dystaxia, spastic paralysis,deafness and mental disability, but normal stature,normal or milder decreased function of thyroid gland.

表现为、痉挛性瘫痪、耳聋和智能低下为特征,但身材正常、甲状腺功能正常或轻度减低。

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科学60秒-科学美国人 2022年6月合集

The disorder is known as spino-cerebellar ataxia type 1, or SCA-1.

被称为“脊髓小脑型共济失调1型(SCA-1)”。

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Osmosis-

These mutations result in degenerative changes in the cerebellum and often in the spinal cord which causes progressive problems with coordination and balance known as ataxia.

这些突变导致小脑和脊髓的退行改变,这会导致进行运动协调障碍、平衡障碍等,称为共济失调

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实习医生格蕾 第2季

He has fever, sweats, tingling in his lips, fingers and toes, mood swings and lack of coordination.

他有发热,出汗,舌、手指、脚趾麻木,感情绪波动和共济失调

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Osmosis-遗传

If this happens, it causes Angelman syndrome, which results in severe intellectual diability, seizures, and ataxia.

如果此基因突变,则导致安格尔曼综合征,患者出现重的智力残、癫痫和共济失调

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Osmosis-

Motor symptoms can include muscle weakness, muscle spasms, tremors, and ataxia, which is a loss of balance and coordination.

运动症状包括肌无力、肌痉挛、震颤和共济失调(失去平衡和协调运动)。

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Osmosis-

In fact, many different gene mutations have been identified each of which is known to cause different types of spinocerebellar ataxia.

实际上,目前已鉴定出不同的基因突变;每突变都会导致不同类型的脊髓小脑共济失调

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Osmosis-

Alright as a quick recap, spinocerebellar ataxia is a group of progressive neurodegenerative diseases of genetic origin.

得!快速回顾一下~脊髓小脑共济失调是一组遗传进行退行

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Buzzfeed 女时尚杂谈

[Morgan] Everything is kinda difficult for me, but because I have Friedreich's ataxia, which is a type of muscular dystrophy.

因为我患有弗里德赖希氏共济失调,这是一肌肉萎缩症。

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科学60秒-科学美国人 2022年7月合集

Her work with Harry is already being used in clinical trials for treating SCA-1 and other disorders.

霍尔:她与哈里合作的研究已应用于治疗脊髓小脑共济失调1型及其他的相关临床试验中。

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Anime Out of Context

The one I just read is, uh, an Ataxaphobic class president who is also Rentaro's cousin.

我刚读到的是一个患有共济失调恐惧症的班长,同时也是莲太郎的表亲。

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科学60秒-科学美国人 2022年7月合集

Huda says this collaboration has deepened their knowledge not just of SCA-1, but other neurological disorders, like Alzheimer's and Parkinson's disease.

霍尔:胡达说这次合作不仅加深了他们对脊髓小脑共济失调1型的了解,还涉及到了其他,比如阿尔茨海默和帕金森

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科学60秒-科学美国人 2022年7月合集

They typically die around 20 years later, of causes related to breathing or swallowing problems. The disorder is known as spino-cerebellar ataxia type 1, or SCA-1.

他们通常在大约20年后因呼吸或吞咽问题相关的因去世。这被称为脊髓小脑共济失调1型,或简称SCA-1。

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科学60秒-科学美国人 2022年7月合集

Between them, they've discovered that the gene responsible for SCA-1 produces a protein called ATAXIN-1 that causes clumps in the brain and leads to that loss of balance.

霍尔:他们共同发现,导致脊髓小脑共济失调1型的基因会产生一名为共济失调蛋白1的蛋白质,这蛋白质会在大脑中形成团块,从而导致平衡能力丧失。

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科学60秒-科学美国人 2022年7月合集

Eventually, Huda found a mistake in the data from the family she was studying—everyone had assumed a group of daughters had inherited SCA-1 from their mother.

霍尔:最终,胡达在她研究的家庭数据中发现了一个错误—— everyone had assumed 这群女儿都从她们的母亲那里继承了脊髓小脑共济失调1型。

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科学60秒-科学美国人 2022年7月合集

With the samples Huda gathered and the help of her colleagues, she discovered that the gene responsible for SCA-1 was located on chromosome 6.

霍尔:在胡达收集的样本和同事的帮助下,她发现导致脊髓小脑共济失调1型的基因位于6号染色体上。

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