Evidence map›Paper›PMID 42071822›Full record

ReviewMedicine2026

A novel mutation in the human RAX gene in patients with microphthalmia and coloboma: A case report and literature review.

Zhangyi Li, Shurui Ke, Wenjuan Wan, Ji Sun, Ke Hu, Can Li

Abstract readCase ReportsReview
In one paragraph

Review in Medicine, 2026. 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

6 authors.

Zhangyi LiDepartment of Ophthalmology, Chongqing Emergency Medical Center, Chongqing University Center Hospital, The Fourth People's Hospital of Chongqing, Chongqing, China.ORCID 0000-0002-0329-6367
Shurui KeDepartment of Ophthalmology, The First Affiliated Hospital of Chongqing Medical University; Chongqing Key Lab of Ophthalmology; Chongqing Eye Institute, Chongqing, China.
Wenjuan WanDepartment of Ophthalmology, The First Affiliated Hospital of Chongqing Medical University; Chongqing Key Lab of Ophthalmology; Chongqing Eye Institute, Chongqing, China.
Ji SunDepartment of Ophthalmology, The First Affiliated Hospital of Chongqing Medical University; Chongqing Key Lab of Ophthalmology; Chongqing Eye Institute, Chongqing, China.
Ke HuDepartment of Ophthalmology, The First Affiliated Hospital of Chongqing Medical University; Chongqing Key Lab of Ophthalmology; Chongqing Eye Institute, Chongqing, China.
Can LiDepartment of Ophthalmology, The First Affiliated Hospital of Chongqing Medical University; Chongqing Key Lab of Ophthalmology; Chongqing Eye Institute, Chongqing, China.ORCID 0000-0003-0481-5218

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleMicrophthalmia, anophthalmia, and coloboma (MAC) form a spectrum of severe developmental eye anomalies. Reports of human MAC associated with RAX mutations remain limited, exhibiting substantial phenotypic heterogeneity. Clinically managing these ocular anomalies or investigating their genetic mechanisms continues to present significant challenges. PATIENT CONCERNS: A 28-year-old female and her 2 sisters L and Q presented with lifelong poor vision, ocular examination revealed similar phenotype among them, including narrow palpebral fissures, bilateral ptosis with epicanthus and esotropia, small cornea, iris coloboma and microspherophakia with uneven lens opacity, in addition to irreversible low vision. DIAGNOSES: Based on ocular examination, the proband was diagonosised with microphthalmia and coloboma, and her 2 sisters were diagonosised with coloboma. WES detected a novel RAX mutation in the 3 affected siblings.

interventionsCataract extraction surgeries combined with complicate scleral fixation of intraocular lens were performed bilaterally in the proband and unilaterally in the right eyes of patient L and Q. OUTCOMES: The proband demonstrated improved bilateral visual acuity postoperatively, reaching 20/125 and 20/100. Patient Q's right eye achieved 20/200 visual acuity, while Patient L's right eye showed no change. The corrected intraocular pressure in Patient L's right eye maintained below 21 mm Hg without requiring antiglaucoma medication. LESSONS: The clinical management of MAC remains challenging. Identifying pathogenic genes could enable curative approaches for this condition. In pediatric patients with visual impairment, prompt intervention targeting ocular and systemic complications proves essential for optimizing visual outcomes.

Indexed as

ColobomaEye ProteinsHomeodomain ProteinsMicrophthalmosMutationTranscription FactorsAdultCataract ExtractionFemaleHumansPedigreePhenotypeEye ProteinsHomeodomain ProteinsRAX protein, humanTranscription FactorscolobomamicrophthalmiamutationRAX

Identifiers

PMID42071822
PMCPMC13124414

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.