作者: Neerupma Singh Akhilesh tiwari* , Kamlesh Dashora , Neelima Salvi
DOI:
关键词:
摘要: Huntington's disease is a complex degenerative disorder that affects the central nervous system. an autosomal-dominant, progressive neurodegenerative typically presents during mid-life with distinct phenotype, including chorea and dystonia, incoordination, cognitive decline, behavioural difficulties. Attempts to study early are not unique in neurology (e.g., mild impairment vascular impairment), but studying otherwise healthy-appearing individuals who have nearly 99% certainty of manifesting symptoms brain does provide valuable information about true natural history disease. The review aims majorly on four areas namely: mehanisms, features, treatment other aspects Huntington’s