ArticleBMC ophthalmology2025
Bilateral vision loss as first clinical manifestation of IgA nephropathy.
Article in BMC ophthalmology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundImmunoglobulin A nephropathy (IgAN) is the most common primary glomerular disease, characterized by IgA deposition in the renal glomeruli. Its clinical manifestations range from asymptomatic hematuria to progressive chronic kidney disease (CKD), with rare cases presenting as nephrotic syndrome or rapidly progressive glomerulonephritis. The eye involvement could be present with a various spectrum of clinical presentation, unusually as first presentation and isolated. CASE PRESENTATION: A 30-year-old male presented to the emergency department with rapidly progressive bilateral visual loss over two days. He had a history of mild upper respiratory symptoms treated with ibuprofen and a known history of asthma. Ophthalmologic evaluation revealed significant retinal findings, including hemorrhages, cotton wool spots, macular edema, and neurosensory detachment. His blood pressure was markedly elevated at 200/140 mmHg, prompting systemic evaluation. Laboratory tests revealed acute kidney injury with elevated creatinine and proteinuria. Renal ultrasound indicated cortical hyperechogenicity, and a renal biopsy confirmed IgAN with mesangial IgA deposition. After antihypertensive treatment and stabilization of renal function, the patient’s vision and retinal findings improved significantly over three weeks. DISCUSSION: This case illustrates an uncommon presentation of IgAN with acute hypertensive crisis manifesting initially only as bilateral visual impairment. The retinal findings, including Roth spots and choroidal involvement, highlight the importance of ophthalmic evaluation in systemic diseases. Although hypertensive retinopathy is well documented, its association with IgAN is rarely reported in literature, especially as first manifestation.
conclusionsIgAN can present atypically with isolated ocular symptoms, underscoring the need for a comprehensive multidisciplinary approach. Clinicians should consider systemic evaluation in patients with hypertensive retinopathy and acute visual loss to facilitate early diagnosis and management of underlying renal pathology.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.