Longitudinally Extensive Spinal Cord Lesion in Leber's Hereditary Optic Neuropathy Due to the M.3460A Mitochondrial DNA Mutation Longitudinally Extensive Spinal Cord Lesion in Leber's Hereditary Optic Neuropathy due to the M.3460A Mitochondrial DNA Mutation (.pdf)

Faisal Y. Althekair, Amy A. Pruitt, Laura O'Keefe, Madhura A. Tamhankar

Publication date

February 2016

Publisher

Spencer S. Eccles Health Sciences Library, University of Utah

Abstract

Leber's hereditary optic neuropathy (LHON) is an inherited mitochondrial disorder characterized by optic nerve degeneration leading to progressive visual loss. Prior reports have described multiple sclerosis (MS) associated with all three primary LHON mutations (m.11778A>G, m.3460A>G, and m.14484T>C. Furthermore, neuromyelitis optica (NMO) has been reported in a patient with nt11778 LHON mtDNA mutation

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Longitudinally Extensive Spinal Cord Lesion in Leber's Hereditary Optic Neuropathy Due to the M.3460A Mitochondrial DNA Mutation Longitudinally Extensive Spinal Cord Lesion in Leber's Hereditary Optic Neuropathy due to the M.3460A Mitochondrial DNA Mutation (.pdf)

Abstract

Extracted data

Longitudinally Extensive Spinal Cord Lesion in Leber's Hereditary Optic Neuropathy Due to the M.3460A Mitochondrial DNA Mutation Longitudinally Extensive Spinal Cord Lesion in Leber's Hereditary Optic Neuropathy due to the M.3460A Mitochondrial DNA Mutation (.pdf)

Abstract

Extracted data

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