简介：医疗系统的前景是什么？作为眼科医疗工作者,我们不仅要治疗眼睛,我们更要治疗患者。同样,眼科医疗并非在真空中作业,而是从属于更宽泛的医疗保健系统。当我们的工作需要如此之多的人力之时,很可能让人忘记工作的大背景是什么。然而,

简介：眼科医生经常会遇到手术器械损坏的情况,而又不愿直接把它们丢掉。因此,在基层医院的医生办公室里通常都会存着一大盒的旧眼科器械,希望有一天能有人把它们修理一下重新使用。(图1)

简介：过敏性眼表疾病是眼科门诊常见的眼部炎症。由于眼表暴露在各种各样的过敏原下,使眼部易导致过敏性反应。过敏性眼部疾病最特征的表现是眼部的瘙痒感,表现为双侧性,临床表现因人而异。

简介：儿童盲的诊治是视觉2020的优先治疗区域,因为视力障碍的孩子们将面对的是长达一生的失明。全球各种研究表明,有1/3到1/2的儿童盲是可避免或者可治疗的,白内障是可治疗儿童盲的首位病因。

简介：AIM:ToinvestigatethesideeffectsofthecommonlyusedlasertreatmentalongwithtestingtheneuroprotectiveeffectofbFGFonapotentialretinalimpairment.METHODS:Todothis,30chinchillapigmentedadultmalerabbitsweredividedintothecontrolandexperimentalgroups.ThecontrolandexperimentalgroupsunderwentbothlaserapplicationandbFGFtreatment.Theretinaltissueimpairmentanditsrenewalrateweretestedunderthelightandelectronmicroscopicallevels.RESULTS:Thefocallaserapplicationonrabbiteyescausedmorphologicalalterationsbothintheapplicationregionandintheneighbouringareas.Inthedamagedareas,theouternuclearlayeroftheneuralretinawasalmostdisappeared,retinapigmentepitheliumwasinterrupted,theretinapigmentepitheliummigratedintraretinally,andthedamagedregionalongwithneighbouringareasseemedtobenotseparated.bFGFapplicationjustafterthelaserphotocoagulation,revealedbetterresultsinapplicationareas.CONCLUSION:ItcouldbesuggestedthatthebFGFapplicationfollowinglaserphotocoagulationmighthaveprotective,repairingandwoundhealingeffectsontheretina.

简介：AIM:ToidentifythegeneticdefectinaChinesefamilywithbilateralprogressivechildhoodposteriorcataract.METHODS:Atwo-generationfamilywasrecruitedinthisstudy.Familyhistoryandclinicaldatawererecorded.AllreportedcandidategenesassociatedwithcongenitalposteriorcataractwerescreenedbydirectDNAsequencing.·RESULTS:Allaffectedindividualspresentedposterioropacitiesinthelens.Directsequencingofthecandidategenesshowedaheterozygousc.2668C>TvariationinEPHA2gene,whichresultedinthereplacementofargininebycysteineatcodon890(p.R890C).Thismutationwasfoundintwoaffectedindividuals,butwasnotobservedin200normalcontrols.·CONCLUSION:Wereportanovelmutation(p.R890C)intheEPHA2receptortyrosinekinasegene.ThefindingexpandsthemutationspectrumofEPHA2inassociationwithposteriorcataract.