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Letter to the Editor

Med Arch. 2018; 72(3): 234-236


Broad Phenotypic Heterogeneity and Multisystem Involvement in Single mtDNA Deletion-associated Pearson Syndrome

Josef Finsterer, Fulvio A. Scorza, Carla A. Scorza.

Abstract
We read with interest the article by Khasawneh et al. about a 4 months-old male with Pearson syndrome due to a novel mtDNA deletion (1). We have the following comments and concerns.

Key words: Pearson Syndrome, mtDNA






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The articles in Bibliomed are open access articles licensed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License (https://creativecommons.org/licenses/by-nc-sa/4.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.