A case report of Multi System Atrophy (MSA) with cross over features of Progressive Supranuclear Palsy (PSP)

R. Judah Rajendran, Kannan Ramesh, Prasanth Hannah Ranjee
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Abstract

Multi System Atrophy is a rare neurodegenerative, synucleinopathic disorder which progresses rapidly. It often presents with symptoms similar to Parkinsonism posing a diagnostic dilemma. It is an orphan disease with an annual incidence of 0.1 to 3 per 100,000, with many being revealed only on autopsy, following years of treatment for Parkinson’s disease. There are very few cases reported from India, possibly because diagnosis requires a high index of suspicion, coupled with a comprehensive knowledge of the disease in order to detect it early and prevent progression.
进行性核上性麻痹(PSP)伴多系统萎缩1例
摘要多系统萎缩是一种罕见的神经退行性、突触性疾病,其进展迅速。它通常表现出与帕金森症相似的症状,使诊断陷入困境。这是一种孤儿病,年发病率为每10万人0.1至3人,其中许多人只有在对帕金森病进行多年治疗后才在尸检中发现。印度报告的病例很少,可能是因为诊断需要高度的怀疑指数,再加上对疾病的全面了解,以便及早发现并防止进展。
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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