Congenital Retinal Vascular Anomalies-1 (Hereditary Retinal Artery Tortuosity, Congenital Retinal Macrovessel, Congenital Retinal Fold, Combined Hamartoma)

نویسندگان

چکیده

Congenital vascular anomalies of the retina are rare, but they should be evaluated with a multidisciplinary approach because can associated systemic diseases and cause severe vision loss. This article aimed to review literature about retinal tortuosity, macrovessel, congenital folds, combined hamartoma.

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منابع مشابه

[Congenital retinal macrovessel: case report].

The authors report a case of arteriolar retinal macrovessel, diagnosed by routine ophthalmologic examination, as well as its optic coherence tomography aspects. Congenital retinal macrovessel is a large aberrant vessel, often unilateral, usually a vein, rarely an artery, located in the posterior pole which can cross the fovea and median raphe.

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Congenital retinal macrovessel: a case report.

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Central serous chorioretinopathy in a patient with congenital retinal macrovessel.

An otherwise healthy 46-year-old man complained with sudden visual loss and a black spot in his left eye. The patient referred a recent stressful episode and was not using corticosteroids. Best-corrected visual acuity was 20/20 and 20/40 in the right eye and left eye, respectively. Applanation tonometry and anterior segment examination of both eyes were unremarkable. Fundus examination of the l...

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Multiple retinal hemorrhages in bilateral congenital venous tortuosity

We present a case of a previously healthy 52-year-old woman with acute onset of scotomas in both eyes. It was associated with headache and vomiting for the past 1 week after a cold. The best-corrected visual acuity was 20/20 in both eyes. The examination of bilateral fundus revealed a venous tortuosity and mild dilatation in the posterior pole, with pre- and intraretinal hemorrhages. However, v...

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Congenital simple hamartoma of the retinal pigment epithelium.

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ژورنال

عنوان ژورنال: Güncel retina

سال: 2023

ISSN: ['2564-7156', '2548-0693']

DOI: https://doi.org/10.37783/crj-0354