Myopia management
Build repeat-use workflows around progression tracking, atropine awareness, and chair-side monitoring for school-age patients.
Concise clinical summaries focused on recognition, differential diagnosis, and referral thresholds — grouped by anatomical region for quick access.
This section is broad, so the priority is practical detection support rather than trying to make every disease page equally exhaustive. Higher-value conditions should connect directly to pathways, tools, and reference pages.
If you are triaging where to spend time, these four clusters are the best places to connect disease recognition with pathways, calculators, and medication-awareness references.
Build repeat-use workflows around progression tracking, atropine awareness, and chair-side monitoring for school-age patients.
Link workup, severity grading, medication-awareness, and ocular surface differentials so clinicians can move faster from symptoms to plan.
Keep risk stratification, co-management, and medication-awareness close together for repeat use in monitoring and referral decisions.
Use cataract content mainly for recognition, documentation, peri-operative awareness, and referral-ready slit-lamp findings.
Keratitis, keratoconus, ulcers, dystrophies, and ocular surface disease.
Open categoryUveitis, aniridia, melanoma, hyphema, pigment dispersion, and angle disorders.
Open categoryAMD, diabetic retinopathy, occlusions, detachment, and inherited disorders.
Open categoryBlepharitis, trichiasis, ptosis, lid lesions, and eyelid malignancies.
Open categoryConjunctivitis, allergic disease, pterygium, episcleritis, and ocular surface neoplasia.
Open categorySevere protozoal infection, often contact lens-related with ring infiltrate.
Leading cause of central vision loss in older adults — dry and wet forms.
Bilateral itch and chemosis from IgE-mediated mast cell degranulation; managed with antihistamines.
Congenital near-total iris absence from PAX6 mutation; associated with glaucoma, foveal hypoplasia, and WAGR syndrome.
Anterior chamber cells and flare with ciliary flush; most common uveitis type — urgent slit-lamp diagnosis required.
Chronic bilateral disease in adults with atopic dermatitis; risk of fornix scarring and corneal neovascularisation.
Anterior segment dysgenesis with posterior embryotoxon and iris strands; ~50% develop glaucoma.
Mucopurulent discharge with diffuse injection; usually self-limiting, topical antibiotics shorten duration.
Most common eyelid malignancy, locally invasive with pearly borders.
Chronic inflammation of the eyelid margins, often staphylococcal or meibomian-related.
Involuntary bilateral orbicularis oculi spasm causing functional blindness; idiopathic or dystonia-related.
Sudden sectoral vision loss from arterial embolus or thrombosis.
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