1- Neurological Department, Krankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Austria.
2- University of Tunis El Manar and Genomics Platform, Pasteur Institute of Tunis, Tunisia.
Abstract:
We read with interest the article by Almasi et al. on a 48 years old female patient with Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-like episodes (MELAS), diagnosed based on the clinical presentation, blood test results, and imaging and muscle biopsy findings . We have the following comments and concerns.
Type of Study:
Commentary |
Subject:
Clinical Neuroscience Received: 2017/11/26 | Accepted: 2019/03/11 | Published: 2020/07/14