2018
DOI: 10.1080/09273948.2018.1500612
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Fuchs’ Uveitis in Iranian Patients: A Review of 89 Eyes

Abstract: Heterochromia is an infrequent clinical feature in Iranian FU patients, however, vitreous involvement is common. Intermediate uveitis is a usual misdiagnosis.

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Cited by 14 publications
(16 citation statements)
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“…However, the presenting speci c signs and symptoms may be subtle and misdiagnosis of FU remains a common clinical problem. [4][5][6][7] Even though heterochromia is a common characteristic nding in patients from Western European descent, it is much less common in patients from other ethnicities. However, regardless of ethnic differences, characteristic iris atrophic changes, other than heterochromia, are common in FU and are key to the correct diagnosis in many cases.…”
Section: Introductionmentioning
confidence: 99%
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“…However, the presenting speci c signs and symptoms may be subtle and misdiagnosis of FU remains a common clinical problem. [4][5][6][7] Even though heterochromia is a common characteristic nding in patients from Western European descent, it is much less common in patients from other ethnicities. However, regardless of ethnic differences, characteristic iris atrophic changes, other than heterochromia, are common in FU and are key to the correct diagnosis in many cases.…”
Section: Introductionmentioning
confidence: 99%
“…However, regardless of ethnic differences, characteristic iris atrophic changes, other than heterochromia, are common in FU and are key to the correct diagnosis in many cases. 7 With the advent of anterior segment optical coherence tomography (AS-OCT), some investigators attempted to quantitatively study these atrophic changes; mostly by introducing various methods to measure iris thickness in AS-OCT images. However, the results are mixed.…”
Section: Introductionmentioning
confidence: 99%
“…14 Whereas clinical FUS landmarks (heterochromia) can be missed in adult, especially those with dark irides, 15,16 or with bilateral diseases. 17 Furthermore, corticosteroids are ineffective and deleterious, hastening the occurrence of cataract and glaucoma. 8 Thus, FUS and RVAU misdiagnoses lead to inappropriate management and iatrogenic complications.…”
Section: Introductionmentioning
confidence: 99%
“…Most cases manifest with characteristic fine stellate keratic precipitates (Fuchs KPs), mild anterior chamber reaction, iris atrophic changes, vitreous cells and debris, posterior subcapsular cataract, glaucoma, absence of macular edema, and absence of posterior synechiae. [4, 5] Despite the well-known clinical picture, incorrect diagnosis of FU is still a frequent problem. [4, 5]…”
Section: Introductionmentioning
confidence: 99%
“…[4, 5] Despite the well-known clinical picture, incorrect diagnosis of FU is still a frequent problem. [4, 5]…”
Section: Introductionmentioning
confidence: 99%