CornOrb: A Multimodal Dataset of Orbscan Corneal Topography and Clinical Annotations for Keratoconus Detection
Authors: Mohammed El Amine Lazouni, Leila Ryma Lazouni, Zineb Aziza Elaouaber, Mohammed Ammar, Sofiane Zehar, Mohammed Youcef Bouayad Agha, Ahmed Lazouni, Amel Feroui, Ali H. Al-Timemy, Siamak Yousefi, Mostafa El Habib Daho
Organizations: Biomedical Engineering Laboratory, Abou Bakr Belkaid University, Tlemcen, Algeria · LIST Laboratory, M’Hamed Bougara Boumerdes University, Algeria · Lazouni Clinic, Tlemcen, Algeria · College of Excellence, University of Baghdad, Iraq · Bascom Palmer Eye Institute, University of Miami, USA · University of Western Brittany, LaTIM UMR1101, Inserm, Brest, France
In this paper, we present CornOrb, a publicly accessible multimodal dataset of Orbscan corneal topography images and clinical annotations collected from patients in Algeria. The dataset comprises 1,454 eyes from 744 patients, including 889 normal eyes and 565 keratoconus cases. For each eye, four corneal maps are provided (axial curvature, anterior elevation, posterior elevation, and pachymetry), together with structured tabular data including demographic information and key clinical parameters such as astigmatism, maximum keratometry (Kmax), central and thinnest pachymetry, and anterior/posterior asphericity. All data were retrospectively acquired, fully anonymized, and pre-processed into standardized PNG and CSV formats to ensure direct usability for artificial intelligence research. This dataset represents one of the first large-scale Orbscan-based resources from Africa, specifically built to enable robust AI-driven detection and analysis of keratoconus using multimodal data. The data are openly available at Zenodo.
Figures & tables
Figure 1: Representative Orbscan 3 corneal maps included in the CornOrb dataset: (a) axial curvature, (b) anterior elevation, (c) posterior elevation, and (d) pachymetry. Each map is standardized to a resolution of 560×560 pixels and saved in PNG format.
Figure 2: Schematic representation of the CornOrb dataset structure. Data are organized hierarchically by patient (from 001 to 744) and eye (OD = right eye, OS = left eye). Each eye includes four Orbscan 3 corneal maps. A CSV file accompanies the images with demographic and clinical annotations. Note: D = diopters, the standard unit for refractive power and keratometry.
Variable name
Unit / Type
Description
patient_code
string
Unique pseudonymized identifier assigned to each patient.
sex
categorical (M/F)
Patient sex.
age
years (integer)
Age at examination.
eye
categorical (OD/OS)
Eye laterality: OD = right eye, OS = left eye.
astigmatism_D
diopters (float)
Magnitude of corneal astigmatism.
astigmatism_axis
degrees (0–180)
Axis of astigmatism.
Table 1: Data dictionary for the clinical_annotations.csv file.
Variable
Normal (n=889)
Keratoconus (n=565)
pBH
Age (years)
33.5±7.4
27.9±7.1
<0.001
Central pachymetry ( μ m)
530±43
465±54
<0.001
Thinnest pachymetry ( μ m)
521±44
427±59
<0.001
K max (D)
43.7±2.9
53.1±6.9
<0.001
Astigmatism (D)
−1.35±0.91
−5.32±3.32
<0.001
Anterior asphericity
−0.15±0.45
−1.20±0.81
<0.001
Table 2: Summary statistics with one additional column reporting the BH-adjusted p -value for the Normal vs. Keratoconus comparison.
Figure 3: Distributions of quantitative clinical measures by diagnosis (Normal vs. Keratoconus). Panels display age (years), K max (D), central pachymetry ( μ m), astigmatism (D), and anterior/posterior asphericity (dimensionless). Colors: Normal (blue), Keratoconus (red).
Figure 4: The Bausch & Lomb Orbscan 3 device used for all corneal topography acquisitions in the CornOrb dataset.
Medical image benchmarks compare AI methods on curated clinical images, tasks, and evaluation protocols to measure accuracy, robustness, and clinical usefulness.
While deep learning has advanced automated glaucoma screening via color fundus photography, existing purely data-driven models often overfit to confounding imaging artifacts and struggle to capture unpredictable pathological cues located beyond predefined anatomical boundaries. To address these limitations, we propose a retinal knowledge-oriented framework that synergizes dynamic multi-scale feature learning with domain-specific anatomical priors. The proposed architecture adopts a tri-branch structure to jointly model the global retinal context, the structural characteristics of the optic cup and disc, and dynamically cropped pathological regions. Specifically, we devise a Dynamic Window Mechanism (DWM) that adaptively discovers diagnostically informative patches via image-level supervision. Furthermore, we introduce a Knowledge-Enhanced Convolutional Block Attention Module (KE-CBAM) that explicitly incorporates retinal priors from a pre-trained foundation model RETFound to guide spatial attention, preventing the network from assigning spurious weights to irrelevant background noise. Extensive evaluations on the large-scale AIROGS dataset demonstrate that our method achieves a state-of-the-art AUC of 98.5% and an accuracy of 94.6%. More importantly, the integration of anatomical priors effectively mitigates the inherent class imbalance, significantly improving the detection of referable glaucoma cases. Additional validations on the SMDG-19 benchmark further confirm its superior cross-domain generalization, indicating that our contribution provides a robust, interpretable, and scalable solution for real-world clinical glaucoma diagnosis. Our code is available at https://github.com/magiczhuo/Glaucoma-Detection
Chi Liu, Yuzhuo Zhou, Sheng Shen +9
Faculty of Data Science, City University of Macau, Avenida Padre Tomás Pereira, Taipa, 999078, Macao, China · State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Vision Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou, 510000, Guangdong, China · Hainan International College, Minzu University of China, Li’an International Education Innovation Pilot Zone, Lingshui, 572423, Hainan, China +4
Background: Artificial intelligence (AI)-based glaucoma detection from colour fundus photographs (CFP) offers scalable screening, but performance may decline on external datasets because of differences in ground-truth definitions, populations, and coexisting conditions such as high myopia (HM). We developed and validated a Vision Transformer-based deep learning (DL) model for glaucoma detection across multi-ethnic cohorts with and without HM. Methods: A ViT-B/16 model with predictive uncertainty estimation was developed using 56,483 CFPs (57.1% with myopia; 14.4% with HM). Glaucoma labels were standardised using clinical, imaging, and perimetry data. The model was validated on 16 independent datasets across three continents, including four datasets with explicit HM labels. Findings: Internal AUROC was 98.7% (95% CI 98.2-99.1%), with sensitivity 94.5% and specificity 97.3%. Across 16 external datasets from eight countries, AUROCs ranged from 86.4% to 99.6%. In HM eyes, internal AUROC was 97.8% (95% CI 96.1-99.2%), with sensitivity 94.8% and specificity 93.7%. External HM AUROCs were 86.5% in the Beijing Eye Study and 93.3%, 91.8%, and 85.5% in hospital-based datasets from Taiwan, Thailand, and South Korea. In an exploratory HM clinical evaluation, the model had higher CFP-only diagnostic accuracy than ophthalmologists and trained graders (92.0% vs 70.0%; p=0.008) and performed comparably to glaucoma specialists using full clinical information. Interpretation: The model showed robust glaucoma detection across myopic and non-myopic multi-ethnic populations and may support AI-assisted screening in settings with high HM prevalence.
Raghavan Lavanya, Yangqin Feng, Ten Cheer Quek +36
Singapore Eye Research Institute, Singapore National Eye Centre, Singapore · Ophthalmology & Visual Sciences Academic Clinical Program (Eye ACP), Duke-NUS Medical School, Singapore · Institute of Advanced Intelligence and Computing, Agency for Science, Technology and Research, Singapore +14
Accurate segmentation of corneal layers in optical coherence tomography (OCT) is essential for quantitative assessment of corneal morphology, including layer thickness and structural changes associated with disease or surgery. However, automatic segmentation remains challenging because corneal interfaces are thin, affected by speckle noise, and variable across acquisition devices. In this work, we propose ARCOS, a patch-based zero-shot boundary localization framework for corneal layer segmentation in clinical anterior-segment OCT images. Rather than performing conventional region classification, the method predicts boundary heatmaps for the main corneal interfaces from overlapping native-resolution patches. Patch-level predictions are stitched across the full B-scan and converted into boundary locations to obtain continuous, anatomically ordered layer segmentations. The network combines multi-scale feature fusion with a self-conditioned refinement module that uses intermediate boundary information to improve local heatmap predictions while preserving spatial detail. The method was evaluated on clinical OCT images acquired from multiple devices and compared with representative segmentation baselines using boundary localization and derived thickness metrics. The proposed method achieved an off-by-one boundary localization accuracy of 95.1% and a mean absolute boundary error of 0.514 pixels on the matched-device test set. In zero-shot cross-device evaluation, it maintained an average off-by-one accuracy of 84.3% and a mean absolute boundary error of 0.855 pixels across unseen acquisition devices, outperforming the baseline models. Thickness estimates derived from the predicted boundaries showed low error across corneal regions, supporting the method's use for quantitative corneal OCT analysis.
Nuno Vivas Brás, Benjamin Memmi, Maëlle Bouhassane +4
Laboratoire d’Optique et Biosciences, CNRS, INSERM, ´Ecole polytechnique, Institut Polytechnique de Paris, Palaiseau, France · GRC 32, Transplantation et Th´erapies Innovantes de la Corn´ee, Sorbonne Universit´e, Centre Hospitalier National d’Ophtalmologie des Quinze-Vingts, Paris, France