Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy

• LHON cases can show brainstem lesions without visual impairment. • There can be inconsistency between MRI finding and clinical symptom in LHON cases. • Auditory pathways may be often involved in LHON cases.

Detalles Bibliográficos
Autores principales: Miyaue, Noriyuki, Yamanishi, Yuki, Tada, Satoshi, Ando, Rina, Yabe, Hayato, Nagai, Masahiro, Nomoto, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348755/
https://www.ncbi.nlm.nih.gov/pubmed/30705974
http://dx.doi.org/10.1016/j.ensci.2019.01.002
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author Miyaue, Noriyuki
Yamanishi, Yuki
Tada, Satoshi
Ando, Rina
Yabe, Hayato
Nagai, Masahiro
Nomoto, Masahiro
author_facet Miyaue, Noriyuki
Yamanishi, Yuki
Tada, Satoshi
Ando, Rina
Yabe, Hayato
Nagai, Masahiro
Nomoto, Masahiro
author_sort Miyaue, Noriyuki
collection PubMed
description • LHON cases can show brainstem lesions without visual impairment. • There can be inconsistency between MRI finding and clinical symptom in LHON cases. • Auditory pathways may be often involved in LHON cases.
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spelling pubmed-63487552019-01-31 Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy Miyaue, Noriyuki Yamanishi, Yuki Tada, Satoshi Ando, Rina Yabe, Hayato Nagai, Masahiro Nomoto, Masahiro eNeurologicalSci Case Report • LHON cases can show brainstem lesions without visual impairment. • There can be inconsistency between MRI finding and clinical symptom in LHON cases. • Auditory pathways may be often involved in LHON cases. Elsevier 2019-01-11 /pmc/articles/PMC6348755/ /pubmed/30705974 http://dx.doi.org/10.1016/j.ensci.2019.01.002 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Miyaue, Noriyuki
Yamanishi, Yuki
Tada, Satoshi
Ando, Rina
Yabe, Hayato
Nagai, Masahiro
Nomoto, Masahiro
Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
title Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
title_full Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
title_fullStr Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
title_full_unstemmed Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
title_short Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
title_sort repetitive brainstem lesions in mitochondrial dna 11778g>a mutation of leber hereditary optic neuropathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348755/
https://www.ncbi.nlm.nih.gov/pubmed/30705974
http://dx.doi.org/10.1016/j.ensci.2019.01.002
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