Eye Diseases, Hereditary

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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
MeSH Number(s)	C11.270 C16.320.290
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".

Diseases [C]
Eye Diseases [C11]
Eye Diseases, Hereditary [C11.270]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Eye Diseases, Hereditary [C16.320.290]

Below are MeSH descriptors whose meaning is related to "Eye Diseases, Hereditary".

Below are MeSH descriptors whose meaning is more specific than "Eye Diseases, Hereditary".

publications

Timeline | Most Recent

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.

Bar chart showing 9 publications over 5 distinct years, with a maximum of 4 publications in 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1997	1	0	1
2013	1	0	1
2016	1	1	2
2020	1	0	1
2021	1	3	4

Below are the most recent publications written about "Eye Diseases, Hereditary" by people in Profiles.

Jivraj I, Cruz CA, Pistilli M, Kohli AA, Liu GT, Shindler KS, Avery RA, Garvin MK, Wang JK, Ross A, Tamhankar MA. 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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Farazdaghi MK, Trimboli-Heidler C, Liu GT, Garcia A, Ying GS, Avery RA. Utility of Ultrasound and Optical Coherence Tomography in Differentiating Between Papilledema and Pseudopapilledema in Children. J Neuroophthalmol. 2021 12 01; 41(4):488-495.

View in: PubMed
Kohli AA, Pistilli M, Alfaro C, Ross AG, Jivraj I, Bagchi S, Chan J, May D, Liu GT, Shindler KS, Tamhankar MA. Role of Ocular Ultrasonography to Distinguish Papilledema From Pseudopapilledema. J Neuroophthalmol. 2021 06 01; 41(2):206-211.

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Reggie SN, Avery RA, Bavinger JC, Jivraj I, Alfaro C, Pistilli M, Kohli AA, Liu GT, Shindler KS, Ross AG, Kardon RH, Sibony PA, Tamhankar M. 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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Chang MY, Binenbaum G, Heidary G, Morrison DG, Galvin JA, Trivedi RH, Pineles SL. Imaging Methods for Differentiating Pediatric Papilledema from Pseudopapilledema: A Report by the American Academy of Ophthalmology. Ophthalmology. 2020 10; 127(10):1416-1423.

View in: PubMed
Feldman S, Peterseim MMW, Trivedi RH, Edward Wilson M, Cheeseman EW, Papa CE. Detecting High Hyperopia: The Plus Lens Test and the Spot Vision Screener. J Pediatr Ophthalmol Strabismus. 2017 May 01; 54(3):163-167.

View in: PubMed
Kramer GD, Say EA, Shields CL. 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.

View in: PubMed
McClelland C, Walsh RD, Chikwava KR, Johnson MP, Mattei P, Liu GT. Congenital mydriasis associated with megacystis microcolon intestinal hypoperistalsis syndrome. J Neuroophthalmol. 2013 Sep; 33(3):271-5.

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Kerrison JB, Maumenee IH. Neuro-ophthalmic genetics. Curr Opin Ophthalmol. 1997 Dec; 8(6):35-40.

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