Abstract
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a maternally inherited genetic mitochondrial disease with a typical onset in the first two decades of life and a major involvement of central nervous system (CNS). We present the case of a man affected with an oligosymptomatic, genetically determined MELAS syndrome, whose clinical picture dramatically and irreversibly worsened following a mild head injury. We hypothesize that the CNS metabolic stress induced by the brain injury activated an irreversible cascade of events leading to progressive neurodegeneration because damaged mitochondria were unable to restore the balance between energy requirements and availability.
Funder
the Italian Ministry of Health
Subject
Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference16 articles.
1. Mitochondrial DNA 3243A>T mutation in a patient with MELAS syndrome;Ikeda;Hum. Genome Var.,2018
2. Mitochondrial DNA mutation “m.3243A>G”-Heterogeneous clinical picture for cardiologists (“m.3243A>G”: A phenotypic chameleon);Niedermayr;Congenit. Heart Dis.,2018
3. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome;Pavlakis;Ann. Neurol.,1984
4. Adam, M.P., Everman, D.B., Mirzaa, G.M., Pagon, R.A., and Wallace, S.E. (2001). GeneReviews®, University of Washington.
5. CT and MR of MELAS syndrome;Ailard;Am. J. Neuroradiol.,1988
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献