"Retinoschisis" 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.
A vitreoretinal dystrophy characterized by splitting of the neuroretinal layers. It occurs in two forms: degenerative retinoschisis and X chromosome-linked juvenile retinoschisis.
| Descriptor ID |
D041441
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| MeSH Number(s) |
C11.768.585.865
|
| Concept/Terms |
Retinoschisis, Juvenile, X-Linked- Retinoschisis, Juvenile, X-Linked
- Retinoschisis, Juvenile, X Chromosome-Linked
- Retinoschisis, X-Linked
- Retinoschises, X-Linked
- Retinoschisis, X Linked
- X-Linked Retinoschises
- Retinoschisis X-Linked Juvenile
- Juvenile, Retinoschisis X-Linked
- Juveniles, Retinoschisis X-Linked
- Retinoschisis X Linked Juvenile
- Retinoschisis X-Linked Juveniles
- X-Linked Juvenile, Retinoschisis
- X-Linked Juveniles, Retinoschisis
- X-Linked Retinoschisis
- X Linked Retinoschisis
- Congenital X-Linked Retinoschisis
- Retinoschisis, Juvenile
- Juvenile Retinoschises
- Juvenile Retinoschisis
- Retinoschises, Juvenile
- X-Linked Juvenile Retinoschisis
- Juvenile Retinoschises, X-Linked
- Juvenile Retinoschisis, X-Linked
- Retinoschises, X-Linked Juvenile
- Retinoschisis, X-Linked Juvenile
- X Linked Juvenile Retinoschisis
- X-Linked Juvenile Retinoschises
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Below are MeSH descriptors whose meaning is more general than "Retinoschisis".
Below are MeSH descriptors whose meaning is more specific than "Retinoschisis".
This graph shows the total number of publications written about "Retinoschisis" by people in this website by year, and whether "Retinoschisis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2020 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Retinoschisis" by people in Profiles.
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A Spontaneous Nonhuman Primate Model of Myopic Foveoschisis. Invest Ophthalmol Vis Sci. 2023 Jan 03; 64(1):18.
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Predominant Founder Effect among Recurrent Pathogenic Variants for an X-Linked Disorder. Genes (Basel). 2022 04 12; 13(4).
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Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome". Ophthalmic Genet. 2021 02; 42(1):100.
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Retinoschisis associated with Kearns-Sayre syndrome. Ophthalmic Genet. 2020 10; 41(5):497-500.