{"title":"绒毛膜视网膜缺损:临床表现、并发症及治疗选择","authors":"A. Altıntaş","doi":"10.15406/aovs.2019.09.00357","DOIUrl":null,"url":null,"abstract":"Choroio Retinal coloboma (CRC) characterized by congenital absence of part of the retinal pigment epithelium and choroid, caused by the defective closure of the embryonic fissure, which normally develops gradually between sixth and seventh weeks of fetal life. Colobomas present various parts of ocular tissue such as iris and /or uvea, lens, optic nerve or eyelid. Since it is embriological pathology CRC may also be associated with other ocular pathologies such as cataract, microphthalmia, anophthalmia.1−4","PeriodicalId":90420,"journal":{"name":"Advances in ophthalmology & visual system","volume":"19 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Chorioretinal coloboma: clinical presentation complications and treatment alternatives\",\"authors\":\"A. Altıntaş\",\"doi\":\"10.15406/aovs.2019.09.00357\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Choroio Retinal coloboma (CRC) characterized by congenital absence of part of the retinal pigment epithelium and choroid, caused by the defective closure of the embryonic fissure, which normally develops gradually between sixth and seventh weeks of fetal life. Colobomas present various parts of ocular tissue such as iris and /or uvea, lens, optic nerve or eyelid. Since it is embriological pathology CRC may also be associated with other ocular pathologies such as cataract, microphthalmia, anophthalmia.1−4\",\"PeriodicalId\":90420,\"journal\":{\"name\":\"Advances in ophthalmology & visual system\",\"volume\":\"19 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-08-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in ophthalmology & visual system\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15406/aovs.2019.09.00357\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in ophthalmology & visual system","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/aovs.2019.09.00357","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Chorioretinal coloboma: clinical presentation complications and treatment alternatives
Choroio Retinal coloboma (CRC) characterized by congenital absence of part of the retinal pigment epithelium and choroid, caused by the defective closure of the embryonic fissure, which normally develops gradually between sixth and seventh weeks of fetal life. Colobomas present various parts of ocular tissue such as iris and /or uvea, lens, optic nerve or eyelid. Since it is embriological pathology CRC may also be associated with other ocular pathologies such as cataract, microphthalmia, anophthalmia.1−4
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