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Updated: Jun 27, 2026

Assessment of Open Probability of the Mitochondrial Permeability Transition Pore in the Setting of Coenzyme Q Excess
Published on: June 1, 2022
Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: a case report
Raquel Montero1, Jose A Sánchez-Alcázar, Paz Briones
1Department of Clinical Biochemistry, Hospital Sant Joan de Déu, Barcelona, Spain.
Objectives:
To report on a case with a mitochondrial DNA (mtDNA) depletion syndrome.
Design And Methods:
Laboratory studies were done in muscle biopsy and fibroblasts to evaluate coenzyme Q(10) (CoQ(10)) status and quantify mitochondrial DNA.
Results:
Decreased CoQ(10) values and a 78% of mtDNA depletion were detected in muscle. Mutational studies failed to reveal any pathogenic mutation in nuclear genes related with mtDNA maintenance.
Conclusions:
mtDNA depletion syndrome was associated with CoQ(10) deficiency in our patient.
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