Evidence map›Paper›PMID 38345780›Full record

ReviewInternational ophthalmology2024

Fuchs endothelial corneal dystrophy: an updated review.

Francisco Altamirano, Gustavo Ortiz-Morales, Mario A O'Connor-Cordova, Juan Pablo Sancén-Herrera, Judith Zavala, Jorge E Valdez-Garcia

Abstract readReview
PubMed Publisher
In one paragraph

Review in International ophthalmology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
11.3field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 28 citations in OpenAlex.

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  11. Molecular Studies ofInternational journal of molecular sciences · 2025
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  12. Review
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  16. From Genes to Disease: ReassessingInternational journal of molecular sciences · 2025
    Article
  17. Article
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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.

Francisco AltamiranoTecnologico de Monterrey, School of Medicine and Health Sciences, Monterrey, Mexico.ORCID http://orcid.org/0000-0003-4587-6201
Gustavo Ortiz-MoralesTecnologico de Monterrey, School of Medicine and Health Sciences, Monterrey, Mexico.ORCID http://orcid.org/0000-0003-4217-8985
Mario A O'Connor-CordovaTecnologico de Monterrey, School of Medicine and Health Sciences, Monterrey, Mexico.ORCID http://orcid.org/0000-0002-3731-5984
Juan Pablo Sancén-HerreraTecnologico de Monterrey, School of Medicine and Health Sciences, Monterrey, Mexico.ORCID http://orcid.org/0009-0001-9689-121X
Judith ZavalaTecnologico de Monterrey, School of Medicine and Health Sciences, Monterrey, Mexico.ORCID http://orcid.org/0000-0002-6116-5816
Jorge E Valdez-GarciaTecnologico de Monterrey, School of Medicine and Health Sciences, Monterrey, Mexico. jorge.valdez@tec.mx.ORCID http://orcid.org/0000-0001-8828-720X
Tecnológico de Monterrey · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe present review will summarize FECD-associated genes and pathophysiology, diagnosis, current  therapeutic approaches, and future treatment perspectives.

methodsLiterature review.

resultsFuchs' endothelial corneal dystrophy (FECD) is the most common bilateral corneal dystrophy and accounts for one-third of all corneal transplants performed in the US. FECD is caused by a combination of genetic and non-heritable factors, and there are two types: early-onset FECD, which affects individuals from an early age and is usually more severe, and late-onset FECD, which is more common and typically manifests around the age of 40. The hallmark findings of FECD include progressive loss of corneal endothelial cells and the formation of focal excrescences (guttae) on the Descemet membrane. These pathophysiological changes result in progressive endothelial dysfunction, leading to a decrease in visual acuity and blindness in later stages. The present review will summarize FECD-associated genes and pathophysiology, diagnosis, current therapeutic approaches, and future treatment perspectives.

conclusionWith the characterization and understanding of FECD-related genes and ongoing research into regenerative therapies for corneal endothelium, we can hope to see more significant improvements in the future in the management and care of the disease.

Indexed as

Corneal TransplantationFuchs' Endothelial DystrophyBlindnessEndothelial CellsEndothelium, CornealHumansCorneal dystrophyEyeFuchs’ endothelial corneal dystrophyGeneticsRho kinase inhibitors

Identifiers

PMID38345780
OpenAlexW4391746524

What OpenQuestion holds

Textmetadata
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.