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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
Case study of a challenging diagnostic dilemma
L. monocytogenes endophthalmitis is often difficult to diagnose and requires high clinical suspicion
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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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