A Patient with Multiple System Atrophy-Parkinsonian Type Presenting with Progressive Micrographia

H. Onder, Beyza Nur Cetin, S. Comoglu
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Abstract

Abstract Herein, we present the case of a 57-year-old male patient who was admitted to our center due to progressive writing difficulty and slowness of his right hand over the last 3 years. In conclusion of the clinical and laboratory workup, a diagnosis of multiple system atrophy (MSA) was established. Our report on progressive micrographia (PM) constitutes a crucial sample remarking on this intriguing manifestation in another disease subtype of MSA, which differs from Parkinson's disease in terms of the clinical and pathophysiological processes. We think that further studies are warranted to clarify the significance of this entity in movement disorder in clinical practice and to reveal the underlying neural mechanisms.
一名表现为进行性微小书写障碍的多系统萎缩-帕金森病型患者
摘要 本病例是一名 57 岁的男性患者,因右手在过去 3 年中出现进行性书写困难和迟缓而入住本中心。经过临床和实验室检查,确诊为多系统萎缩(MSA)。我们关于进行性显微书写障碍(PM)的报告构成了一个重要的样本,说明了 MSA 的另一种疾病亚型中的这一有趣表现,它在临床和病理生理过程方面与帕金森病不同。我们认为有必要开展进一步的研究,以明确这一实体在临床运动障碍中的意义,并揭示其潜在的神经机制。
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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