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Titlebook: Manual of Retinal Diseases; A Guide to Diagnosis Carlos A. Medina,Justin H. Townsend,Arun D. Singh Book 2016 Springer International Publish

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樓主: COAX
11#
發(fā)表于 2025-3-23 09:53:24 | 只看該作者
Valsalva RetinopathyValsalva retinopathy: preretinal hemorrhage secondary to a sudden increase in intrathoracic pressure.
12#
發(fā)表于 2025-3-23 17:55:08 | 只看該作者
Solar RetinopathySolar retinopathy, Welder’s maculopathy, foveomacular retinitis, eclipse retinopathy, and solar retinitis
13#
發(fā)表于 2025-3-23 19:30:28 | 只看該作者
Purtscher’s RetinopathyPurtscher’s retinopathy: hemorrhagic and vasoocclusive vasculopathy first described in 1912 as a syndrome of sudden blindness associated with severe head trauma. It is most often seen after trauma but commonly associated with other causes. Also known as angiopathia retinae traumatica.
14#
發(fā)表于 2025-3-23 22:57:49 | 只看該作者
Traumatic Lens DislocationSubluxation – incomplete or partial dislocation of lens
15#
發(fā)表于 2025-3-24 02:43:50 | 只看該作者
16#
發(fā)表于 2025-3-24 10:31:20 | 只看該作者
17#
發(fā)表于 2025-3-24 13:00:02 | 只看該作者
Familial Exudative VitreoretinopathyFamilial exudative vitreoretinopathy (FEVR) is a hereditary condition characterized by failure of vascular development of the temporal retina causing peripheral retinal ischemia, exudation, neovascularization, temporal dragging, and tractional retinal detachment.
18#
發(fā)表于 2025-3-24 15:21:53 | 只看該作者
19#
發(fā)表于 2025-3-24 20:19:03 | 只看該作者
ColobomaColoboma is a developmental abnormality with defects of one or several ocular structures. Defects of the eyelids, cornea, iris, ciliary body, zonules, lens, retina, choroid, and/or optic nerve may be present and are caused by incomplete closure of the embryonic fissure.
20#
發(fā)表于 2025-3-24 23:17:38 | 只看該作者
Juvenile X-Linked RetinoschisisJuvenile X-linked retinoschisis is a hereditary disorder characterized by foveal schisis affecting males early in life. Schisis or splitting of the retina’s neurosensory layers in the periphery can also be seen in some cases.
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