学科分类
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4 个结果
  • 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。

  • 标签: 白内障 儿童 盲/预防与控制 统计学 国家健康计划
  • 简介:3.加强县级综合医院眼科能力建设,发挥其作为基层防盲治盲技术指导中心的作用。鼓励城市三级医院眼科、眼科医院与县级综合医院眼科建立紧密的合作关系,通过技术指导、人员培训等方式,使县级综合医院眼科具备常见眼病诊治和急诊处理能力,落实双向转诊。

  • 标签: 防盲治盲 县级综合医院 眼科医院 急诊处理能力 能力建设 三级医院
  • 简介:AIM:Toinvestigatethetreatmentstatusandprognosisofspace-occupyinglacrimalglandlesionsatonetertiaryeyecenterinChina.·METHODS:Aretrospectiveclinicalstudywasperformedon95patientswithspace-occupyinglesionsofthelacrimalglandsurgicallytreatedattheEye&ENTHospitalofFudanUniversityfrom2003to2007.Thereviewedclinicaldataincludedage,gender,sideofthelesion,durationofsignsandsymptoms,histopathologicaldiagnosis,treatmentmodality,recurrence(local,regional,anddistantmetastasis)andsurvival.·RESULTS:Ofthe95cases(99eyes),pleomorphicadenomaswerethemostcommonlesions(43cases),followedbylymphoiddisorders(14),inflammatorypseudotumors(11),carcinomaex-pleomorphicadenomas(11),andadenoidcysticcarcinomas(ACC,6).Therewere8patientswithrelapsedpleomorphicadenomas.Fiveofthese8caseshadmalignantpathologicalchanges.AllpatientswithACChadmetastasisandthreeofthemdiedduringtheirfollow-up.·CONCLUSION:Ourstudyindicatedthatthemostcommonlacrimalglandlesionswerepleomorphicadenomas.Multiplerecurrenceandsurgicalproceduresmayincreasetheriskoftumorprogression.ACChadahighincidenceoftumormetastasisandapoorprognosis.

  • 标签: LACRIMAL GLAND lesions PLEOMORPHIC ADENOMAS ADENOID
  • 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.

  • 标签: EPHA2 gene MUTATION POSTERIOR CATARACT