脊髓小脑共济失调的基因突变与治疗

Camila da Luz Eltchechem, Jéssica Wouk, Luiz Augusto da Silva
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引用次数: 0

摘要

小脑疾病和紊乱导致速度、幅度和力量不足。在小脑功能障碍中,脊髓小脑共济失调是一种以进行性小脑共济失调为特征的病理。脊髓小脑性共济失调的最初临床表现为平衡和协调能力的恶化,除了视力障碍,伴有构音障碍、吞咽困难和锥体和锥体外体征的进行性体位振荡。小脑共济失调是由小脑紊乱及其连接引起的,在先天性和遗传性共济失调的情况下,这可能是由根本原因引起的。本文简要介绍了小脑功能的历史概况,并讨论了一种特殊的小脑功能障碍,脊髓小脑共济失调,强调其生理学,以便更好地理解该疾病,其临床和几种类型的病理。
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Genetic Mutations and Treatment of Spinocerebellar Ataxias
Cerebellar diseases and disturbs cause speed, amplitude and strength deficiency. Among cerebellar dysfunctions, the spinocerebellar ataxia is a pathology characterized by the presence of progressive cerebellar ataxia. Spinocerebellar ataxia has as its initial clinic manifestations the deterioration of equilibrium and coordination, beyond eye disturbances, progressive postural oscillation associated with dysarthria, dysphagia and pyramidal and extrapyramidal signs. Cerebellar ataxias are caused by a cerebellum disorder and its connections, which may be attributed by root causes in the cases of congenital and hereditary ataxias. This review brings a brief historical perspective about cerebellar functions and in addition, a discussion about a specific cerebellar dysfunction, spinocerebellar ataxia, emphasizing its physiology to a better comprehension of the disease, its clinic and the several types of this pathology.
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