Successful treatment of a patient with mitochondrial myopathy with alirocumab.
Sign Up to like & getrecommendations! Published in 2020 at "Journal of clinical lipidology"
DOI: 10.1016/j.jacl.2020.07.007
Abstract: A 48-year-old man presented to our lipid clinic with statin intolerance and elevated serum creatine kinase levels, being affected by mitochondrial myopathy because of heteroplasmic mitochondrial DNA missense mutation in MTCO1 gene (m.7671T>A). He had… read more here.
Keywords: myopathy alirocumab; successful treatment; patient mitochondrial; mitochondrial myopathy ... See more keywords
Brain atrophy in a patient with mitochondrial DNA G8363A mutation
Sign Up to like & getrecommendations! Published in 2019 at "Chinese Medical Journal"
DOI: 10.1097/cm9.0000000000000395
Abstract: The patient’s clinical symptoms improved after treatment To the Editor: Mitochondrial diseases are a common group of human genetic diseases that can occur at any with vitamins, lipoic acid, and coenzymes. However, he decade of… read more here.
Keywords: dna g8363a; dna; patient mitochondrial; brain atrophy ... See more keywords