Evidence map›Paper›PMID 31908405›Full record

ReviewMolecular vision2019

Sector retinitis pigmentosa: Report of ten cases and a review of the literature.

Razek Georges Coussa, Diana Basali, Akiko Maeda, Meghan DeBenedictis, Elias I Traboulsi

Open access · greenAbstract readCase ReportsReview
In one paragraph

Review in Molecular vision, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Observational
  2. Article
  3. Article
  4. Atypical presentation of sector retinitis pigmentosa.Arquivos brasileiros de oftalmologia · 2025
    Article
  5. Article
  6. Rhodopsin mislocalization drives ciliary dysregulation in a novel autosomal dominant retinitis pigmentosa knock-in mouse model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. EYS-Associated Sector Retinitis Pigmentosa.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Razek Georges CoussaCenter for Genetic Eye Diseases, Cole Eye Institute, Cleveland Clinic, Cleveland, OH.
Diana BasaliCenter for Genetic Eye Diseases, Cole Eye Institute, Cleveland Clinic, Cleveland, OH.
Akiko MaedaDepartment of Ophthalmology & Visual Sciences, Case Western Reserve University School of Medicine, Cleveland, OH.
Meghan DeBenedictisCenter for Genetic Eye Diseases, Cole Eye Institute, Cleveland Clinic, Cleveland, OH.
Elias I TraboulsiCenter for Genetic Eye Diseases, Cole Eye Institute, Cleveland Clinic, Cleveland, OH.
Cleveland Eye Clinic · USCase Western Reserve University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To describe the genotypes and phenotypes of ten patients with sector retinitis pigmentosa (RP). We also review previously reported mutations associated with sector RP and provide a discussion of possible underlying pathophysiological mechanisms. Methods: Patients underwent detailed ophthalmologic examinations, fundus photography, fundus autofluorescence (FAF) imaging, spectral-domain optical coherence tomography (SD-OCT), as well as visual field and electroretinographic testing. All patients underwent genetic testing to identify the molecular etiology of their disease. Results: A total of ten patients were studied. Among these patients, nine had mutations in Conclusions: Sector RP is an uncommon form of RP in which only one or two retinal quadrants display clinical pathological signs. The great majority of cases result from mutations in

Indexed as

Amino Acid SequenceAnimalsHumansMutationPhenotypeRetinitis PigmentosaRhodopsinVisual FieldsRhodopsin

Identifiers

PMID31908405
PMCPMC6937219
OpenAlexW3001029992

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.