Evidence map›Paper›PMID 35756836›Full record

ArticleAmerican journal of ophthalmology case reports2022

Retinal dystrophies: A look beyond the eyes.

Vincent Duong Tang, Alena Egense, Glenn Yiu, Elijah Meyers, Ala Moshiri, Suma P Shankar

Open access · goldAbstract readCase Reports
In one paragraph

Article in American journal of ophthalmology case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% of its field
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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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 at 1 institution in 1 country.

Vincent Duong TangDivision of Genomic Medicine, MIND Institute, Department of Pediatrics, UC Davis Medical Center, 2825 50th Street, Sacramento, CA, 95817, USA.
Alena EgenseDivision of Genomic Medicine, MIND Institute, Department of Pediatrics, UC Davis Medical Center, 2825 50th Street, Sacramento, CA, 95817, USA.
Glenn YiuDepartment of Ophthalmology & Visual Sciences, UC Davis Medical Center, 4860 Y St Suite 2400, Sacramento, CA, 95817, USA.
Elijah MeyersDivision of Genomic Medicine, MIND Institute, Department of Pediatrics, UC Davis Medical Center, 2825 50th Street, Sacramento, CA, 95817, USA.
Ala MoshiriDepartment of Ophthalmology & Visual Sciences, UC Davis Medical Center, 4860 Y St Suite 2400, Sacramento, CA, 95817, USA.
Suma P ShankarDivision of Genomic Medicine, MIND Institute, Department of Pediatrics, UC Davis Medical Center, 2825 50th Street, Sacramento, CA, 95817, USA.
University of California Davis Medical Center · US

Funding

The Role of ARAP1 in Retinal Photoreceptor HomeostasisK08EY027463 · NEI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MOSHIRI, ALA · 2017 to 2021
$1.0M
NEI NIH HHS K08 EY027463
6 · The paper itself

Abstract

Purpose: To illustrate the importance of systemic evaluation in retinal dystrophies through examples of Alstrom syndrome, Bardet Biedl syndrome, and Refsum disease. Observations: Detailed eye evaluations, including visual acuity, visual field, slit lamp examination, and indirect ophthalmoscopy were performed. Retinal imaging included fundus photography and spectral domain optical coherence tomography (SD-OCT). Functional testing of the retina was done using full field electroretinography (ffERG). In addition, molecular genetic testing was performed using a ciliopathy panel, a retinal dystrophy panel, and whole genome sequencing (WGS).We report three individuals who presented with vision concerns first to ophthalmology, noted to have retinal dystrophy, and then referred to genomic medicine for genetic testing. Additional evaluation led to suspicion of specific groups of systemic disorders and guided appropriate genetic testing. The first individual presented with retinal dystrophy, obesity, and short stature with no reported neurocognitive deficits. Genetic testing included a ciliopathy panel that was negative followed by WGS that identified biallelic variants in Conclusions and importance: In individuals who present with retinal dystrophy to ophthalmologists, additional systemic manifestations such as sensorineural hearing loss, anosmia, or polydactyly, should be sought and a positive history or examination finding should prompt an immediate referral to a clinical geneticist for additional evaluation and appropriate genetic testing. This facilitates pre-test genetic counseling and allows for more accurate diagnosis, prognosis, and management of affected individuals along with better recurrence risk estimates for family members. Identification of an underlying etiology also enhances the understanding of the pathophysiology of disease and expands the genotypic and phenotypic spectrum. Ultimately, successful recognition of these diseases facilitates development of targeted therapies and surveillance of affected individuals.

Indexed as

Alstrom syndromeBardet Biedl syndromeGenetic testingGenome sequencingRefsum diseaseRetinal dystrophies

Identifiers

PMID35756836
PMCPMC9228281
OpenAlexW4283075101

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.