Leber optic hereditary neuropathy plus dystonia

Rev Neurol (Paris). 2019 Sep-Oct;175(7-8):483-484. doi: 10.1016/j.neurol.2018.12.011. Epub 2019 Jun 17.

Authors

S Mahoui¹, O Belkhamsa², I Ait Kaci³, M Abada Bendib³, G Castelnovo⁴

Affiliations

¹ Department of neurology, university hospital of Ben Aknoun, Algiers, Algeria. Electronic address: mahoui.soulaimane@gmail.com.
² Department of neurology, university hospital Nedir Mohamed, Tizi Ouzou, Algeria.
³ Department of neurology, university hospital of Ben Aknoun, Algiers, Algeria.
⁴ Department of neurology, university hospital of Nîmes, Nîmes, France.

PMID: 31221418
DOI: 10.1016/j.neurol.2018.12.011

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adolescent
Brain / diagnostic imaging
DNA, Mitochondrial / genetics*
Dystonia / etiology
Equinus Deformity / etiology
Humans
Magnetic Resonance Imaging
Male
Mutation*
Optic Atrophy, Hereditary, Leber / complications
Optic Atrophy, Hereditary, Leber / genetics*
Phenotype
Putamen / diagnostic imaging
Vision Disorders / etiology
Visual Acuity

Substances

DNA, Mitochondrial