ReviewInternational journal of molecular sciences2026
Ocular Manifestations in Patients with Werner Syndrome.
Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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.
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Who cites it
1 citing paper in PubMed.
- Global challenges for lens and cataract research.Frontiers in ophthalmology · 2026Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Werner syndrome is a rare autosomal recessive premature aging syndrome characterized by its development after puberty and death in patients in their 50s due to cancer or atherosclerotic disease. Early diagnosis can improve the management of disease, quality of life and prolong the lifespan of patients with Werner syndrome. Ophthalmologists should include Werner syndrome in the general work-up in patients with bilateral early-onset cataracts. We present a case of Werner syndrome with initial signs of juvenile cataracts. The patient had a high-pitched voice, a bird-like face and progeroid hair. We performed routine ophthalmological examinations including slit-lamp examinations, fundus examinations, and optical coherence tomography, and genetic analysis. The patient had plateau iris and pachychoroid-like features in addition to bilateral cataracts. The gene analysis revealed compound heterozygosity of
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