Related to Cerebellar ataxia:cerebellar atrophy a·tax·i·a (ə-tăk′sē-ə) n. 1.Loss of the ability to coordinate muscular movement. 2.Any of various degenerative, often hereditary, disorders that are characterized by ataxia and are frequently associated with cerebellar atrophy. ...
Spinal-cerebellar-ataxias网络脊髓小脑共济失调;小脑脊髓干运动失调网络释义 1. 脊髓小脑共济失调 ...(Huntington disease)、不同类型脊髓小脑共济失调(spinal cerebellar ataxias)、肌萎缩侧索硬化症(amyotrophic lateral sclerosi…www.healthoo.com|基于3个网页 2. 小脑脊髓干运动失调 ... 萎缩症(myotonic dystrophy...
Spinal cerebellar ataxia 11 (SCA11) is a rare disease, characterized by progressive cerebellar ataxia, abnormal eye sign. Four families have been reported in the past. We report on China's first family with spinocerebellar ataxia 11. A careful investigation of the clinical manifestations, brain ...
答案是,并非同一种。 蔡磊先生是渐冻症(Amyotrophic Lateral Sclerosis, ALS),而木藤亚也是脊髓小脑性共济失调(Spinal Cerebellar Ataxia, SCA)。 我们可以简单粗暴得理解为,它们目前都是疑难杂症,都属于无法根治的慢性、进行性的疾病。 两者有一定的相似之处,但确实也存在很多差异。 一、相似点 1. 神经系统疾病:...
Clinical Perspective and Overview of Spinal Cord Disorders and Cerebellar Ataxias. Evidence‐Based Neurological Disorders. Jenny Stanford Publishing; 2024. pp. 229–66. Cascino G and Monteleone AMJP. Early traumatic experiences and the hypothalamus-pituitary-adrenal axis in people with eating disorders:...
have a cerebellum with distinct hemispheric structures (the neocerebellum) that receives information primarily from the cerebral cortex and the visual and acoustic receptors. The degree of cerebellar development varies mainly with the level of development of motor activity. Therefore, in mobile animals ...
Location of the spinal cerebellar ataxia 2 locus to a 1 cM interval on chromsome 12q23-24.1 来自 Semantic Scholar 喜欢 0 阅读量: 17 作者:Allotey, R,Twells, R,Orozco, G 摘要: Spinocerebellar ataxia 2 (SCA2) is a dominantly inherited neurodegenerative disorder characterised by progressive ...
ataxia with infantile onset olivopontocerebellar atrophy atrophia Atrophy calcaneocavus foot Charcot-Marie-Tooth disease circumscribed cerebral atrophy Déjerine-Thomas syndrome disuse atrophy Duchenne-Aran disease gyrate atrophy of choroid and retina juvenile spinal muscular atrophy Kugelberg-Welander syndrome ...
(M1)46or to the spinal cord51. Thus, it can be argued that the PrePMd is anatomically more similar to areas of the prefrontal cortex38, with which it is closely interconnected47,48. Neurophysiology studies in nonhuman primates and neuroimaging studies in humans also support a functional ...
Previous implications have shown that the alterations of the levels of TNF-α in the serum and/or in the cere- brospinal fluid are associated with various brain diseases in human41,42. For example, pro-inflammatory cytokines including TNF-α have been reported to be elevated in psychiatric ...