Published September 2020
| Version v1
Journal article
Neuroimaging research progress in Leber hereditary optic neuropathy
Creators
- 1. Department of Radiology, Tianjin Medical University General Hospital, Tianjin (China)
- 2. School of Medical Imaging, Tianjin Medical University, Tianjin (China)
Description
Leber hereditary optic neuropathy (LHON) is a hereditary neurological disorder characterized by point mutation in mitochondrial DNA, which cause progressive painless vision loss. Recently, imaging techniques such as optical coherence tomography and magnetic resonance imaging have been used to detect the neuronal damages caused by LHON, which provides potential imaging biomarkers for the prevention and treatment of LHON. This paper systematically reviews the latest neuroimaging progress about the damage of the anterior visual pathway and brain tissues. (authors)
Additional details
Identifiers
Publishing Information
- Journal Title
- International Journal of Medical Radiology
- Journal Volume
- 43
- Journal Issue
- 5
- Journal Page Range
- p. 529-533
- ISSN
- 1674-1897
INIS
- Country of Publication
- China
- Country of Input or Organization
- China
- INIS RN
- 55086990
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANIMAL TISSUES; BIOLOGICAL MARKERS; BRAIN; DAMAGE; DNA; GENE MUTATIONS; MITOCHONDRIA; NMR IMAGING; OPTICS; REVIEWS; TOMOGRAPHY
- Descriptors DEC
- BODY; CELL CONSTITUENTS; CENTRAL NERVOUS SYSTEM; DIAGNOSTIC TECHNIQUES; DOCUMENT TYPES; MUTATIONS; NERVOUS SYSTEM; NUCLEIC ACIDS; ORGANIC COMPOUNDS; ORGANS
Optional Information
- Notes
- 37 refs.; http://dx.doi.org/10.19300/j.2020.Z18141