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.
[Med Arch 2018; 72(3.000): 234-236]

Keywords: Pearson Syndrome, mtDNA

>>Full text PDF        >>[cite source=”doi”]10.5455/medarh.2018.72.234-236[/cite]

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