Evidence map›Paper›PMID 41867372›Full record

ReviewMolecular vision2025

Genetic phenotypic characteristics and inheritance patterns of patients with achromatopsia at a large academic institution and a review of the literature and gene therapies.

Sanjana Molleti, Pedro F Monsalve, Richard N Sather, Jade Y Moon, Jacie Ihinger, Sandra R Montezuma

Abstract readReview
In one paragraph

Review in Molecular vision, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sanjana MolletiDepartment of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, MN.
Pedro F MonsalveDepartment of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, MN.
Richard N SatherDepartment of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, MN.
Jade Y MoonDepartment of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, MN.
Jacie IhingerDepartment of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, MN.
Sandra R MontezumaDepartment of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, MN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Achromatopsia (ACHM) is a cone dysfunction syndrome associated with low color vision, photophobia, and congenital nystagmus. Pathogenic variants in the Methods: This retrospective cohort study examined patients with a genetically confirmed diagnosis of ACHM evaluated at the UMN/M Health IRD clinic between May 2015 and August 2022. Data were collected through UMN's electronic health record system and included information on demographics, history of ocular illness, visual acuity, and diagnostic exam results, such as electroretinogram, fundus autofluorescence, and optical coherence tomography (OCT) imaging. Genetic testing was performed using next-generation sequencing panels of varying sizes, and variants were interpreted according to American College of Medical Genetics guidelines. Results: A total of 21 patients with a genetically confirmed ACHM were included in the study. Most patients were female (67%) and white (76%). The cohort included one pair of twin siblings and one group of three siblings. The median age of genetic testing conducted was 12 years (interquartile range, 12-20 years). One-third of patients had nyctalopia. All patients experienced difficulties with color vision, 20 of 21 (95.2%) had photosensitivity, and 18 of 21 patients reported congenital nystagmus. Diagnostic imaging showed most patients with a normal scotopic response and absent photopic response on electroretinogram, macular hyperfluorescence on fundus autofluorescence, and normal optical coherence tomography imaging. Conclusion: This study contributes to an understanding of the phenotypes and distribution of genetic variants associated with achromatopsia at a single academic institution in the state of Minnesota, particularly those involving the

Indexed as

Color Vision DefectsCyclic Nucleotide-Gated Cation ChannelsGenetic TherapyInheritance PatternsAdolescentAdultChildElectroretinographyFemaleGenetic TestingHumansMaleMutationPhenotypeRetrospective StudiesTomography, Optical CoherenceCNGA3 protein, humanCNGB3 protein, humanCyclic Nucleotide-Gated Cation Channels

Identifiers

PMID41867372
PMCPMC13002551

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.