Ophthalmic surgery, lasers & imaging retina · 2019
Multimodal Retinal Imaging Findings in Williams-Beuren Syndrome.
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Erşan Hatice Bilge Araz, Güven Dilek, Demir Atilla Gökçe, Dirim Ayşe Burcu, Kaçar Hakan, Arslan Doğukan
Аннотация
A 17-year-old male patient diagnosed with Williams-Beuren syndrome presented with a gradual decline in vision in both eyes during a 3-year period. The ophthalmologic examination was notable for numerous loop-shaped tortuous vessels accompanying normal appearing retinal vessels and cystoid macular edema (CME). Mild foveal hypoplasia with a persistence of inner retinal layers was noted on spectral-domain optical coherence tomography (OCT). OCT angiography showed that the abnormal vessels were not retinal vessels but were compatible with prepapillary vascular loops. The CME persisted despite repeated intravitreal bevacizumab treatment. The resolution was observed following an intravitreal triamcinolone acetonide injection. [Ophthalmic Surg Lasers Imaging Retina. 2019;50:514-518.].