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Rare genetic disease diagnosed in a young woman – then two additional patients
Aggressive treatment required to control symptoms and prevent central nervous system decline and vision loss
Sleuthing the cause of retinal pigmentary disease and optic nerve changes
Case study of a challenging diagnostic dilemma
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L. monocytogenes endophthalmitis is often difficult to diagnose and requires high clinical suspicion
Delay in treating fracture with entrapment can cause permanent double vision, other sequelae
Case study: With a constellation of findings, OCTA proves best option in diagnosis
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