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white dot syndromes/angiotensin

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Purpose: To report a case of presumed ocular sarcoidosis initially presenting with features of multiple evanescent white dot syndrome (MEWDS) with atypical optical coherence tomography angiography (OCTA) findings.

The Value of Diagnostic Work-Up in the Evaluation of White Dot Syndromes.

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To determine the diagnostic yield of systemic work-up in white dot syndromes. A retrospective chart review. Eighty-six consecutive patients with a diagnosis of a white dot syndrome were identified. Forty-three had a diagnosis of birdshot chorioretinopathy. Overall, 395 diagnostic tests were

Acute posterior multifocal placoid pigment epitheliopathy as the initial manifestation of sarcoidosis.

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OBJECTIVE To report an undiagnosed case of systemic sarcoidosis manifesting with bilateral acute posterior multifocal placoid pigment epitheliopathy (APMPPE). METHODS A 26-year-old Caucasian man was referred for management of unilateral visual loss together with a paracentral scotoma developing 2

[Clinical profile of presumed and definitive ocular sarcoidosis].

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BACKGROUND Sarcoidosis is an antigen-mediated disease of unknown cause defined by granulomatous inflammation of different organs. OBJECTIVE The aim of this study was to analyze the clinical picture in 26 patients with a definitive and presumed ocular sarcoidosis. METHODS The following tests were
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