Mitochondrial encephalopathy and optic neuropathy due to m.10158 MT-ND3 complex I mutation presenting in an adult patient: Case report and review of the literature

Ivana Vodopivec; Tracey A. Cho; Joseph F. Rizzo; Matthew P. Frosch; Katherine B. Sims

Article

Mitochondrial encephalopathy and optic neuropathy due to m.10158 MT-ND3 complex I mutation presenting in an adult patient: Case report and review of the literature

Neurologist

DOI: 10.1097/NRL.0000000000000084

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Abstract

Introduction: Establishing a diagnosis of mitochondrial disease in adults remains a clinician's challenge. We report a case of syndrome reminiscent of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) in an adult patient who carries m.10158T

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Vodopivec, I., Cho, T. A., Rizzo, J. F., Frosch, M. P., & Sims, K. B. (2016). Mitochondrial encephalopathy and optic neuropathy due to m.10158 MT-ND3 complex I mutation presenting in an adult patient: Case report and review of the literature. Neurologist. Lippincott Williams and Wilkins. https://doi.org/10.1097/NRL.0000000000000084

Mitochondrial encephalopathy and optic neuropathy due to m.10158 MT-ND3 complex I mutation presenting in an adult patient: Case report and review of the literature

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