乳酸性酸中毒
症候群
医学
冲程(发动机)
粒线体疾病
失代偿
脑病
线粒体肌病
重症监护医学
生物信息学
内科学
病理
线粒体DNA
生物
遗传学
机械工程
工程类
基因
作者
Daniele Orsucci,Elena Caldarazzo Ienco,Vincenzo Montano,Gabriele Siciliano,Michelangelo Mancuso
标识
DOI:10.1016/j.phrs.2022.106228
摘要
A mitochondrial stroke-like event is an evolving subacute neurological syndrome linked to seizure activity and focal metabolic brain derangement in a genetically determined mitochondrial disorder. The acronym "MELAS" (mitochondrial encephalopathy associated with lactic acidosis and stroke-like lesions) identifies subjects with molecular, biochemical and/or histological evidence of mitochondrial disorder who experience stroke-like lesions. MELAS is a rare inherited mitochondrial disease linked to severe multiorgan involvement and stress-induced episodes of metabolic decompensation and lactic acidosis. Unfortunately, there are no etiopathogenetic therapies for stroke-like episodes to date, and the treatment is mainly based on anti-epileptic drugs and supportive therapies. This perspective opinion article discusses the current care standards for MELAS patients and revises current and innovative emerging therapies for mitochondrial stroke-like episodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI