Evidence map›Paper›PMID 42599617›Full record

ArticleDocumenta ophthalmologica. Advances in ophthalmology2026

Severe visual impairment as a complication of autism spectrum disorder.

Paulina Horwat, Julia Dezor-Garus, Marta Pawlak, Anna Gotz-Więckowska

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Article in Documenta ophthalmologica. Advances in ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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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

4 authors.

Paulina HorwatDepartment of Ophthalmology, Poznan University of Medical Sciences, Augustyna Szamarzewskiego 84, 61-848, Poznan, Poland. paulina.horwat9@gmail.com.ORCID http://orcid.org/0009-0008-3081-5143
Julia Dezor-GarusDepartment of Ophthalmology, Poznan University of Medical Sciences, Augustyna Szamarzewskiego 84, 61-848, Poznan, Poland.
Marta PawlakDepartment of Ophthalmology, Poznan University of Medical Sciences, Augustyna Szamarzewskiego 84, 61-848, Poznan, Poland.
Anna Gotz-WięckowskaDepartment of Ophthalmology, Poznan University of Medical Sciences, Augustyna Szamarzewskiego 84, 61-848, Poznan, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo report the irreversible vision loss caused by optic neuropathy in a course of a vitamin A deficiency.

methodsElectroretinography (ERG) and pattern visual evoked potentials (PVEP) were used to establish a diagnosis, and to monitor the treatment in a child suffering from poor vision likely as a result of vitamin A deficiency.

resultsA 13-year-old boy presented with eye pain, dryness, itching, photophobia, and decreased vision for the past 4 weeks. His medical history was significant for autism spectrum disorder, anxiety-depressive disorder, and eating disorder-neophobia. His visual acuity was severely impaired, measuring 1.2 LogMAR in the right eye and 1.0 LogMAR in the left eye. Slit lamp examination revealed keratinization of the conjunctiva and multiple punctate epithelial defects of the cornea. Optical coherence tomography (OCT) confirmed keratomalacia. The patient was referred to the Pediatric Gastroenterology Unit for further investigation and found to have severe malnutrition including hypovitaminosis A (< 0.05 μmol/L). Treatment included vitamin A supplementation, 200 000 IU, bandage contact lenses, moxifloxacin, and lubricant eye drops. Although it was impossible to perform ERG on the initial visit because of patients' poor general and ocular condition, full field ERGs showed generalized retinal dysfunction after 12 days of treatment. After 11 months, full field ERGs revealed retinal function within normal limits, but the patient's vision remained poor. Pattern visual evoked potentials (PVEPs) suggested persistent optic nerve dysfunction.

conclusionElectrophysiological assessments, including ERG and (PVEP) were central to establishing an accurate diagnosis in cases where resolution of anterior segment lesions due to keratomalacia did not result in visual improvement. These tests are critical for the identification and monitoring of nutritional optic neuropathy.

Indexed as

ElectrophysiologyKeratomalaciaOptic neuropathy,Vision lossVitamin A deficiencyXerophthalmia

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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.