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亚急性硬化性全脑炎——当前观点

Subacute sclerosing panencephalitis - current perspectives.

作者信息

Jafri Sidra K, Kumar Raman, Ibrahim Shahnaz H

机构信息

Department of Pediatrics and Child Health, Aga Khan University Hospital, Karachi, Pakistan,

出版信息

Pediatric Health Med Ther. 2018 Jun 26;9:67-71. doi: 10.2147/PHMT.S126293. eCollection 2018.

Abstract

Subacute sclerosing panencephalitis is a progressive neurodegenerative disease. It usually occurs 7-10 years after measles infection. The clinical course is characterized by progressive cognitive decline and behavior changes followed by focal or generalized seizures as well as myoclonus, ataxia, visual disturbance, and later vegetative state, eventually leading to death. It is diagnosed on the basis of Dyken's criteria. There is no known cure for subacute sclerosing panencephalitis to date, but it is preventable by ensuring that an effective vaccine program for measles is made compulsory for all children younger than 5 years in endemic countries.

摘要

亚急性硬化性全脑炎是一种进行性神经退行性疾病。它通常在麻疹感染后7至10年发生。临床病程的特点是进行性认知衰退和行为改变,随后出现局灶性或全身性癫痫发作以及肌阵挛、共济失调、视觉障碍,后期进入植物人状态,最终导致死亡。它是根据戴肯标准进行诊断的。迄今为止,亚急性硬化性全脑炎尚无已知的治愈方法,但通过确保在流行国家对所有5岁以下儿童强制实施有效的麻疹疫苗接种计划,可以预防该病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723f/6027681/507b73fd47c4/phmt-9-067Fig1.jpg

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