"Retinal Dysplasia" 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, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
Descriptor ID |
D015792
|
MeSH Number(s) |
C11.250.666 C11.270.660 C11.768.660 C16.131.384.784 C16.320.290.660
|
Concept/Terms |
Retinal Dysplasia- Retinal Dysplasia
- Dysplasia, Retinal
- Dysplasias, Retinal
- Retinal Dysplasias
|
Below are MeSH descriptors whose meaning is more general than "Retinal Dysplasia".
Below are MeSH descriptors whose meaning is more specific than "Retinal Dysplasia".
This graph shows the total number of publications written about "Retinal Dysplasia" by people in this website by year, and whether "Retinal Dysplasia" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2010 | 2 | 0 | 2 |
2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Retinal Dysplasia" by people in Profiles.
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Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature. Am J Med Genet A. 2014 Nov; 164A(11):2879-86.
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Laser photocoagulation at birth prevents blindness in Norrie's disease diagnosed using amniocentesis. Ophthalmology. 2010 Dec; 117(12):2402-6.
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In utero diagnosis of Norrie disease and early laser preserves visual acuity. Arch Ophthalmol. 2010 Oct; 128(10):1382.