Evidence map›Paper›PMID 40950277›Full record

ArticleAmerican journal of translational research2025

Case report of a CRYGS gene mutation in a patient with congenital cataracts and secondary glaucoma.

Wan Li, Fei Chen

Abstract readCase Reports
In one paragraph

Article in American journal of translational research, 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

2 authors.

Wan LiDepartment of Ophthalmology, Union Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology Wuhan 430022, Hubei, China.
Fei ChenDepartment of Ophthalmology, Union Hospital Affiliated to Tongji Medical College of Huazhong University of Science and Technology Wuhan 430022, Hubei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital cataracts are a major cause of visual impairment in infants and young children, with glaucoma being a frequent complication after cataract surgery. Here, we report a case of congenital cataracts accompanied by secondary glaucoma following surgery and we preliminarily investigate the genetic etiology. Comprehensive physical examination was performed, and genomic DNA extracted from the patient's was subjected to exome sequencing. A heterozygous variant of uncertain significance in the

Indexed as

Congenital cataractCRYGS geneexome sequencinggenetic mutationglaucoma

Identifiers

PMID40950277
PMCPMC12432746

What OpenQuestion holds

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Registered trials

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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.