Quantitative Analysis of Iris Changes Following Physiologic and Pharmacologic Mydriasis in Subjects

来源 :第十七届亚非眼科大会暨中华医学会第十九次全国眼科学术大会 | 被引量 : 0次 | 上传用户:zhuxuchen0822
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
Purpose To estimate and compare change in iris crosssectional area (IA) and iris volume (IV) after physiologic and pharmacologic mydriasis in subjects with different mechanisms for primary angle closure using anterior segment optical coherence tomography (AS-OCT) Design Population-based cross-sectional observational study.
其他文献
Purpose There is no consensus as to the optimum treatment for traumatic optic neuropathy (TON).The decision to intervene medically or surgically, or simply observe was recommended to be on an individu
会议
Purpose To describe the technique of endoscopic transethmoidal orbital fat decompression (ETOFD) for proptosis inGraves orbitopathy (GO) and report outcomes.Design: Retrospective, interventional case
会议
Objective: High-velocity trauma to the upper face results in complex orbital fractures, and due to the anatomic position, ophthalmic and neurological complications are encountered as well as sequels o
会议
Objective Primarily screen differentially expressed microRNAs of the TAO groups, compared to control group,via the part of immunopathogenesis.Method Patients were divided into 3 groups,silent TAO grou
会议
Purposes: To study the anatomical characters remaining in the macular after successful idiopathic macular hole surgery using optic coherence tomography (OCT), and further analyze the correlation betwe
会议
Purpose To evaluate the efficacy and safety of multiple intravitreal injections of ganciclovir for patients with cytomegalovirus (CMV) retinitis after stem cell transplantation.
会议
Purpose Leber Congenital Amaurosis (LCA) represents the most severe form of human inherited retinal dystrophies with photoreceptor neuron degeneration and blindness with an incidence of ~1 in 80,000.T
会议
PURPOSE To investigate the clinical phenotypes for Leber congenital amaurosis (LCA) and early-onset severe retinal dystrophy (ESRD) associated with RPE65.
会议
Purpose To identify pathogenic mutations responsible for Usher syndrome (USH) in five unrelated Chinese USH families.Methods Clinical data and genomic DNA were collected for patients with USH and avai
会议
Background Glaucoma is a group of disorders with optic neuropathy.It is characterized by progressive injury to retinal ganglion cells and their axons and causes progressive visual field loss.Glaucoma
会议