Evidence map›Paper›PMID 35566651›Full record

ReviewJournal of clinical medicine2022

Eye Involvement in Wilson's Disease: A Review of the Literature.

Kevin Chevalier, Martine Mauget-Faÿsse, Vivien Vasseur, Georges Azar, Michaël Alexandre Obadia, Aurélia Poujois

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. A diagnostic dilemma in a child with Wilson's disease.Pediatric nephrology (Berlin, Germany) · 2026
    Article
  2. Article
  3. Review
  4. Neuropsychiatric manifestations of Wilson's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. The history of Wilson disease.Clinical liver disease
    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 2 countries.

Kevin ChevalierDepartment of Neurology, Rothschild Foundation Hospital, 75019 Paris, France.ORCID 0000-0001-7823-1827
Martine Mauget-FaÿsseDepartment of Ophthalmology, Rothschild Foundation Hospital, 75019 Paris, France.ORCID 0000-0002-4711-9397
Vivien VasseurClinical Research Center Coordinator, Rothschild Foundation Hospital, 75019 Paris, France.ORCID 0000-0002-7647-3088
Georges AzarDepartment of Ophthalmology, Rothschild Foundation Hospital, 75019 Paris, France.ORCID 0000-0002-9808-5545
Michaël Alexandre ObadiaDepartment of Neurology, Rothschild Foundation Hospital, 75019 Paris, France.ORCID 0000-0002-4221-6163
Aurélia PoujoisDepartment of Neurology, Rothschild Foundation Hospital, 75019 Paris, France.
Fondation de Rothschild · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wilson's disease (WD) is an autosomal recessive genetic disorder due to a mutation of the ATP7B gene, resulting in impaired hepatic copper excretion and accumulation in various tissues. Ocular findings are one of the hallmarks of the disease. Many ophthalmological manifestations have been described and new techniques are currently available to improve their diagnosis and to follow their evolution. We have performed a systematic PubMed search to summarize available data of the recent literature on the most frequent ophthalmological disorders associated with WD, and to discuss the newest techniques used for their detection and follow-up during treatment. In total, 49 articles were retained for this review. The most common ocular findings seen in WD patients are Kayser-Fleischer ring (KFR) and sunflower cataracts. Other ocular manifestations may involve retinal tissue, visual systems and eye mobility. Diagnosis and follow-up under decoppering treatment of these ocular findings are generally easily performed with slit-lamp examination (SLE). However, new techniques are available for the precocious detection of ocular findings due to WD and may be of great value for non-experimented ophthalmologists and non-ophthalmologists practitioners. Among those techniques, anterior segment optical coherence tomography (AS-OCT) and Scheimpflug imaging are discussed.

Indexed as

coppereye involvementKayser–Fleischer ringsunflower cataractWilson’s disease

Identifiers

PMID35566651
PMCPMC9102176
OpenAlexW4225150437

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.