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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
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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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030405060708091011120102
20252026

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