"Eye Abnormalities" 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.
Congenital absence of or defects in structures of the eye; may also be hereditary.
| Descriptor ID |
D005124
|
| MeSH Number(s) |
C11.250 C16.131.384
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Eye Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Eye Abnormalities".
This graph shows the total number of publications written about "Eye Abnormalities" by people in this website by year, and whether "Eye Abnormalities" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 1 | 0 | 1 |
| 2004 | 0 | 2 | 2 |
| 2005 | 1 | 0 | 1 |
| 2006 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2014 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Eye Abnormalities" by people in Profiles.
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Epiglottic aplasia in an infant with Joubert syndrome. BMJ Case Rep. 2020 Nov 09; 13(11).
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Primary Cilia Signaling Promotes Axonal Tract Development and Is Disrupted in Joubert Syndrome-Related Disorders Models. Dev Cell. 2019 12 16; 51(6):759-774.e5.
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Arl13b and the exocyst interact synergistically in ciliogenesis. Mol Biol Cell. 2016 Jan 15; 27(2):308-20.
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Brittle cornea syndrome: a case report and comparison with Ehlers Danlos syndrome. J AAPOS. 2014 Oct; 18(5):509-11.
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Molecular staging of marine medaka: a model organism for marine ecotoxicity study. Mar Pollut Bull. 2011; 63(5-12):309-17.
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Progression of a unilateral posterior lentiglobus associated with a persistent fetal vasculature stalk. J AAPOS. 2010 Feb; 14(1):81-2.
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Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5.
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Eye field requires the function of Sfrp1 as a Wnt antagonist. Neurosci Lett. 2007 Feb 27; 414(1):26-9.
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Iris hypoplasia and aorticopulmonary septal defect: a neurocristopathy. J AAPOS. 2005 Jun; 9(3):264-7.
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POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8.