{"title":"先天性小眼伴眼眶囊肿的研究现状。","authors":"Bei Li","doi":"10.1007/s10792-024-03387-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Purposes: </strong>Congenital microphthalmia with orbital cyst (CMOC) is a severe ocular developmental malformation. This article aims to provide assistance for genetic counseling and further exploration of more effective treatments.</p><p><strong>Methods: </strong>A combined systematic search of PubMed electronic database by using Boolean operators AND and OR was conducted, choosing the following keywords: \"microphthalmos\", \"microphthalmia\", \"cyst\", \"morbidity\", \"congenital cystic eye\", \"histopathological\", \"molecular genetics\", \"syndrome\", \"treatment\", \"therapy\", \"surgery\" and \"surgical\" etc. After the initial screening of these articles, repetitive literatures were excluded.</p><p><strong>Results: </strong>63 articles were selected. This article reviewed the research progress on the incidence of CMOC, its relationship with congenital microphthalmos and congenital cystic eye, histopathology and molecular genetics studies, particularly the syndromes associated with this condition and the current treatment status.</p><p><strong>Conclusion: </strong>CMOC is essentially a disease caused by gene mutations, and there is no effective treatment that achieves consistent relief. Further research to clarify the genotype-phenotype and inheritance patterns of this disease may be a valuable research direction for exploring effective treatment methods and guiding clinical genetic counseling.</p>","PeriodicalId":14473,"journal":{"name":"International Ophthalmology","volume":"45 1","pages":"13"},"PeriodicalIF":1.4000,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Research status of congenital microphthalmos with orbital cyst.\",\"authors\":\"Bei Li\",\"doi\":\"10.1007/s10792-024-03387-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purposes: </strong>Congenital microphthalmia with orbital cyst (CMOC) is a severe ocular developmental malformation. This article aims to provide assistance for genetic counseling and further exploration of more effective treatments.</p><p><strong>Methods: </strong>A combined systematic search of PubMed electronic database by using Boolean operators AND and OR was conducted, choosing the following keywords: \\\"microphthalmos\\\", \\\"microphthalmia\\\", \\\"cyst\\\", \\\"morbidity\\\", \\\"congenital cystic eye\\\", \\\"histopathological\\\", \\\"molecular genetics\\\", \\\"syndrome\\\", \\\"treatment\\\", \\\"therapy\\\", \\\"surgery\\\" and \\\"surgical\\\" etc. After the initial screening of these articles, repetitive literatures were excluded.</p><p><strong>Results: </strong>63 articles were selected. This article reviewed the research progress on the incidence of CMOC, its relationship with congenital microphthalmos and congenital cystic eye, histopathology and molecular genetics studies, particularly the syndromes associated with this condition and the current treatment status.</p><p><strong>Conclusion: </strong>CMOC is essentially a disease caused by gene mutations, and there is no effective treatment that achieves consistent relief. Further research to clarify the genotype-phenotype and inheritance patterns of this disease may be a valuable research direction for exploring effective treatment methods and guiding clinical genetic counseling.</p>\",\"PeriodicalId\":14473,\"journal\":{\"name\":\"International Ophthalmology\",\"volume\":\"45 1\",\"pages\":\"13\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-12-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Ophthalmology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10792-024-03387-0\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Ophthalmology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10792-024-03387-0","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:先天性小眼球伴眶囊肿(CMOC)是一种严重的眼部发育畸形。本文旨在为遗传咨询和进一步探索更有效的治疗方法提供帮助:方法:使用布尔运算符 AND 和 OR 对 PubMed 电子数据库进行联合系统检索,选择以下关键词:"小眼球"、"小眼球症"、"囊肿"、"发病率"、"先天性囊性眼"、"组织病理学"、"分子遗传学"、"综合征"、"治疗"、"疗法"、"手术 "和 "外科 "等。对这些文章进行初步筛选后,排除了重复性文献:结果:共筛选出 63 篇文章。本文综述了 CMOC 的发病率、与先天性小眼症和先天性囊性眼的关系、组织病理学和分子遗传学研究等方面的研究进展,尤其是与该病相关的综合征和治疗现状:结论:CMOC 本质上是一种由基因突变引起的疾病,目前还没有有效的治疗方法可以持续缓解病情。进一步研究阐明该病的基因型-表型和遗传模式,可能是探索有效治疗方法和指导临床遗传咨询的一个有价值的研究方向。
Research status of congenital microphthalmos with orbital cyst.
Purposes: Congenital microphthalmia with orbital cyst (CMOC) is a severe ocular developmental malformation. This article aims to provide assistance for genetic counseling and further exploration of more effective treatments.
Methods: A combined systematic search of PubMed electronic database by using Boolean operators AND and OR was conducted, choosing the following keywords: "microphthalmos", "microphthalmia", "cyst", "morbidity", "congenital cystic eye", "histopathological", "molecular genetics", "syndrome", "treatment", "therapy", "surgery" and "surgical" etc. After the initial screening of these articles, repetitive literatures were excluded.
Results: 63 articles were selected. This article reviewed the research progress on the incidence of CMOC, its relationship with congenital microphthalmos and congenital cystic eye, histopathology and molecular genetics studies, particularly the syndromes associated with this condition and the current treatment status.
Conclusion: CMOC is essentially a disease caused by gene mutations, and there is no effective treatment that achieves consistent relief. Further research to clarify the genotype-phenotype and inheritance patterns of this disease may be a valuable research direction for exploring effective treatment methods and guiding clinical genetic counseling.
期刊介绍:
International Ophthalmology provides the clinician with articles on all the relevant subspecialties of ophthalmology, with a broad international scope. The emphasis is on presentation of the latest clinical research in the field. In addition, the journal includes regular sections devoted to new developments in technologies, products, and techniques.