MELAS or Leigh syndrome, that’s the question

Josef Finsterer

doi:10.5114/pedm.2022.112695

eISSN: 2083-8441
ISSN: 2081-237X

Pediatric Endocrinology Diabetes and Metabolism

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abstract:

Letter to the Editor

MELAS or Leigh syndrome, that’s the question

Josef Finsterer

¹

Klinik Landstrasse, Messerli Institute, Vienna, Austria

Pediatr Endocrinol Diabetes Metab 2021; 27 (4): 311–312

DOI: https://doi.org/10.5114/pedm.2022.112695

Online publish date: 2021/12/30

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With interest we read the article by Baszyńska-Wilk et al. about a 12 years old female who was diagnosed with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome upon the clinical presentation, blood tests, and the cerebral magnetic resonance imaging (MRI) [1]. The diagnosis was neither confirmed by biochemical nor by genetic investigations [1]. The study is appealing but raises the following concerns.

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MELAS or Leigh syndrome, that’s the question

Josef Finsterer 1

MELAS, Leigh syndrome, polyglandular syndrome, lactic acidosis, encephalopathy

Josef Finsterer

¹