"Eye Diseases, Hereditary" 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.
Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
Descriptor ID |
D015785
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MeSH Number(s) |
C11.270 C16.320.290
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Concept/Terms |
Eye Diseases, Hereditary- Eye Diseases, Hereditary
- Disease, Hereditary Eye
- Diseases, Hereditary Eye
- Eye Disease, Hereditary
- Hereditary Eye Disease
- Hereditary Eye Diseases
|
Below are MeSH descriptors whose meaning is more general than "Eye Diseases, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Eye Diseases, Hereditary".
This graph shows the total number of publications written about "Eye Diseases, Hereditary" by people in this website by year, and whether "Eye Diseases, Hereditary" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2016 | 1 | 1 | 2 |
2020 | 1 | 0 | 1 |
2021 | 1 | 3 | 4 |
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Below are the most recent publications written about "Eye Diseases, Hereditary" by people in Profiles.
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Utility of Ultrasound and Optical Coherence Tomography in Differentiating Between Papilledema and Pseudopapilledema in Children. J Neuroophthalmol. 2021 12 01; 41(4):488-495.
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Utility of Spectral-Domain Optical Coherence Tomography in Differentiating Papilledema From Pseudopapilledema: A Prospective Longitudinal Study. J Neuroophthalmol. 2021 12 01; 41(4):e509-e515.
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Role of Ocular Ultrasonography to Distinguish Papilledema From Pseudopapilledema. J Neuroophthalmol. 2021 06 01; 41(2):206-211.
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The sensitivity and specificity of retinal and choroidal folds to distinguish between mild papilloedema and pseudopapilledema. Eye (Lond). 2021 11; 35(11):3131-3136.
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Imaging Methods for Differentiating Pediatric Papilledema from Pseudopapilledema: A Report by the American Academy of Ophthalmology. Ophthalmology. 2020 10; 127(10):1416-1423.
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Detecting High Hyperopia: The Plus Lens Test and the Spot Vision Screener. J Pediatr Ophthalmol Strabismus. 2017 May 01; 54(3):163-167.
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Simultaneous Novel Mutations of LRP5 and TSPAN12 in a Case of Familial Exudative Vitreoretinopathy. J Pediatr Ophthalmol Strabismus. 2016 Feb 04; 53 Online:e1-5.
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Congenital mydriasis associated with megacystis microcolon intestinal hypoperistalsis syndrome. J Neuroophthalmol. 2013 Sep; 33(3):271-5.
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Neuro-ophthalmic genetics. Curr Opin Ophthalmol. 1997 Dec; 8(6):35-40.