"Optic Atrophy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.
| Descriptor ID |
D009896
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| MeSH Number(s) |
C10.292.700.225 C11.640.451
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Optic Atrophy".
Below are MeSH descriptors whose meaning is more specific than "Optic Atrophy".
This graph shows the total number of publications written about "Optic Atrophy" by people in this website by year, and whether "Optic Atrophy" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Optic Atrophy" by people in Profiles.
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Sequelae of neglected hypermature senile cataract. Indian J Ophthalmol. 2019 10; 67(10):1707-1708.
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Microstructure of Parapapillary Atrophy Is Associated With Parapapillary Microvasculature in Myopic Eyes. Am J Ophthalmol. 2018 08; 192:157-168.
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A donor splice site mutation in CISD2 generates multiple truncated, non-functional isoforms in Wolfram syndrome type 2 patients. BMC Med Genet. 2017 12 13; 18(1):147.