"Cone-Rod Dystrophies" 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.
Genetically heterogeneous and sometimes syndromic (e.g., BARDET BIEDL SYNDROME; and SPINOCEREBELLAR ATAXIA TYPE 7) retinopathies with initial RETINAL CONE involvement. They are characterized by decreased VISUAL ACUITY; COLOR VISION DEFECTS; progressive loss of peripheral vision and night blindness.
| Descriptor ID |
D000071700
|
| MeSH Number(s) |
C11.270.152 C11.768.585.658.250 C16.320.290.152
|
| Concept/Terms |
Cone-Rod Dystrophies- Cone-Rod Dystrophies
- Cone Rod Dystrophies
- Retinal Cone-Rod Dystrophy
- Cone-Rod Dystrophies, Retinal
- Cone-Rod Dystrophy, Retinal
- Retinal Cone Rod Dystrophy
- Retinal Cone-Rod Dystrophies
- Cone-Rod Retinal Dystrophy
- Cone Rod Retinal Dystrophy
- Cone-Rod Retinal Dystrophies
- Retinal Dystrophies, Cone-Rod
- Retinal Dystrophy, Cone-Rod
- Cone-Rod Dystrophy
- Cone Rod Dystrophy
- Cone-Rod Degenerations
- Cone Rod Degenerations
- Cone-Rod Degeneration
|
Below are MeSH descriptors whose meaning is more general than "Cone-Rod Dystrophies".
Below are MeSH descriptors whose meaning is more specific than "Cone-Rod Dystrophies".
This graph shows the total number of publications written about "Cone-Rod Dystrophies" by people in this website by year, and whether "Cone-Rod Dystrophies" 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 |
|---|
| 2019 | 1 | 0 | 1 |
| 2020 | 2 | 0 | 2 |
| 2022 | 2 | 0 | 2 |
| 2023 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Cone-Rod Dystrophies" by people in Profiles.
-
RPGR: Deep Phenotyping and Genetic Characterization With Findings Specific to the 3'-end of ORF15. Invest Ophthalmol Vis Sci. 2023 09 01; 64(12):19.
-
Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies. Genes (Basel). 2022 05 22; 13(5).
-
ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease. Invest Ophthalmol Vis Sci. 2022 04 01; 63(4):20.
-
PDE6C: Novel Mutations, Atypical Phenotype, and Differences Among Children and Adults. Invest Ophthalmol Vis Sci. 2020 10 01; 61(12):1.
-
Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort. Am J Med Genet A. 2020 03; 182(3):493-497.
-
Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy. Invest Ophthalmol Vis Sci. 2019 11 01; 60(14):4811-4819.