亨廷顿氏病。临床病例

NATIONAL JOURNAL OF NEUROLOGY Pub Date : 2023-07-30 DOI:10.61788/njn.v1i23.11

R. Shiraliyeva, A. K. Mammadbayli, U. A. Asadova

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引用次数: 0

摘要

亨廷顿氏病是一种影响神经系统白质基底节、尾状核、丘脑、黑质、边缘系统、大脑皮质、小脑的神经退行性疾病，表现为自体显性驱动。早期首发患者的临床病程比传统型更为严重。在缺乏适当对症治疗的情况下，神经系统症状会变得更加严重，表现也更加尖锐。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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HUNTINGTON'S DISEASE. CLINICAL CASE

Huntington's disease is a neurodegenerative disease that affects basal ganglia in the white matter of the nervous system, tailed nucleus, thalamus, black substance, limbic system, cerebral cortex, cerebellum, manifested by autosome-dominant drive. In patients with early debut, the clinical course is more severe than in the classical form. In the absence of proper symptomatic treatment, neurological signs become more severe and sharply expressive.

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NATIONAL JOURNAL OF NEUROLOGY

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