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Analysis of Etiologic Factors in Pediatric Rhegmatogenous Retinal Detachment With Genetic Testing
The purpose of this study was to investigate the etiology and clinical features of nontraumatic rhegmatogenous retinal detachment (RRD) in children. Consecutive, cross-sectional study. In this study, 112 operative eyes of 102 patients ≤18 years of age with nontraumatic RRD were included. Comprehensi...
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Published in: | American journal of ophthalmology 2020-10, Vol.218, p.330-336 |
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description | The purpose of this study was to investigate the etiology and clinical features of nontraumatic rhegmatogenous retinal detachment (RRD) in children.
Consecutive, cross-sectional study.
In this study, 112 operative eyes of 102 patients ≤18 years of age with nontraumatic RRD were included. Comprehensive ophthalmic examinations were performed in all patients. Genetic testing was performed in 34 patients with hereditary congenital/developmental diseases. The etiology of RRD was analyzed.
The average age was 12.2 ± 4.5 years (range, 1-18 years). The percentages of male and female patients were 74.5% (76/102) and 25.5% (26/102), respectively. The most common etiologic factors were congenital/developmental anomalies (51/102, 50%), followed by simple myopia (34/102, 33.3%) and previous intraocular surgery (6/102, 5.9%). More than half (31/51, 60.8%) of the patients with congenital/developmental anomalies had familial exudative vitreoretinopathy. Further analysis of the underlying etiologic factors based on age revealed that the most common etiology of RRD in patients ≤12 years of age was congenital/developmental anomalies (28/48, 58.3%); however, simple myopia was the major etiologic factor in patients >12 years of age (27/54, 50%).
Congenital/developmental diseases were the most common etiologies of pediatric nontraumatic RRD in China. Familial exudative vitreoretinopathy accounted for most of the congenital/developmental anomalies. |
doi_str_mv | 10.1016/j.ajo.2020.02.015 |
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Consecutive, cross-sectional study.
In this study, 112 operative eyes of 102 patients ≤18 years of age with nontraumatic RRD were included. Comprehensive ophthalmic examinations were performed in all patients. Genetic testing was performed in 34 patients with hereditary congenital/developmental diseases. The etiology of RRD was analyzed.
The average age was 12.2 ± 4.5 years (range, 1-18 years). The percentages of male and female patients were 74.5% (76/102) and 25.5% (26/102), respectively. The most common etiologic factors were congenital/developmental anomalies (51/102, 50%), followed by simple myopia (34/102, 33.3%) and previous intraocular surgery (6/102, 5.9%). More than half (31/51, 60.8%) of the patients with congenital/developmental anomalies had familial exudative vitreoretinopathy. Further analysis of the underlying etiologic factors based on age revealed that the most common etiology of RRD in patients ≤12 years of age was congenital/developmental anomalies (28/48, 58.3%); however, simple myopia was the major etiologic factor in patients >12 years of age (27/54, 50%).
Congenital/developmental diseases were the most common etiologies of pediatric nontraumatic RRD in China. Familial exudative vitreoretinopathy accounted for most of the congenital/developmental anomalies.</description><identifier>ISSN: 0002-9394</identifier><identifier>EISSN: 1879-1891</identifier><identifier>DOI: 10.1016/j.ajo.2020.02.015</identifier><identifier>PMID: 32112773</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Age ; Cataracts ; Congenital diseases ; Disease ; Etiology ; Families & family life ; Genetic testing ; Marfan syndrome ; Mutation ; Patients ; Pediatrics ; Retina ; Retinal detachment ; Risk factors ; Surgery</subject><ispartof>American journal of ophthalmology, 2020-10, Vol.218, p.330-336</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><rights>2020. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-a8510288d4562e069b56935c798f5176d6df7fe1883328f50a1cba5cf266ec353</citedby><cites>FETCH-LOGICAL-c381t-a8510288d4562e069b56935c798f5176d6df7fe1883328f50a1cba5cf266ec353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32112773$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Chonglin</creatorcontrib><creatorcontrib>Huang, Sijian</creatorcontrib><creatorcontrib>Sun, Limei</creatorcontrib><creatorcontrib>Li, Songshan</creatorcontrib><creatorcontrib>Huang, Li</creatorcontrib><creatorcontrib>Wang, Zhirong</creatorcontrib><creatorcontrib>Luo, Xiaoling</creatorcontrib><creatorcontrib>Ding, Xiaoyan</creatorcontrib><title>Analysis of Etiologic Factors in Pediatric Rhegmatogenous Retinal Detachment With Genetic Testing</title><title>American journal of ophthalmology</title><addtitle>Am J Ophthalmol</addtitle><description>The purpose of this study was to investigate the etiology and clinical features of nontraumatic rhegmatogenous retinal detachment (RRD) in children.
Consecutive, cross-sectional study.
In this study, 112 operative eyes of 102 patients ≤18 years of age with nontraumatic RRD were included. Comprehensive ophthalmic examinations were performed in all patients. Genetic testing was performed in 34 patients with hereditary congenital/developmental diseases. The etiology of RRD was analyzed.
The average age was 12.2 ± 4.5 years (range, 1-18 years). The percentages of male and female patients were 74.5% (76/102) and 25.5% (26/102), respectively. The most common etiologic factors were congenital/developmental anomalies (51/102, 50%), followed by simple myopia (34/102, 33.3%) and previous intraocular surgery (6/102, 5.9%). More than half (31/51, 60.8%) of the patients with congenital/developmental anomalies had familial exudative vitreoretinopathy. Further analysis of the underlying etiologic factors based on age revealed that the most common etiology of RRD in patients ≤12 years of age was congenital/developmental anomalies (28/48, 58.3%); however, simple myopia was the major etiologic factor in patients >12 years of age (27/54, 50%).
Congenital/developmental diseases were the most common etiologies of pediatric nontraumatic RRD in China. Familial exudative vitreoretinopathy accounted for most of the congenital/developmental anomalies.</description><subject>Age</subject><subject>Cataracts</subject><subject>Congenital diseases</subject><subject>Disease</subject><subject>Etiology</subject><subject>Families & family life</subject><subject>Genetic testing</subject><subject>Marfan syndrome</subject><subject>Mutation</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Retina</subject><subject>Retinal detachment</subject><subject>Risk factors</subject><subject>Surgery</subject><issn>0002-9394</issn><issn>1879-1891</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1rFTEUhoMo9lr9AW4k4MbNjPmYJBNclX4pFJRScRlyM2fuzTAzqUmu0H_vKbe6cOEq5OR53yQPIW85aznj-uPU-im1ggnWMtEyrp6RDe-NbXhv-XOyYYyJxkrbnZBXpUy41aYzL8mJFJwLY-SG-LPVzw8lFppGelljmtMuBnrlQ0250LjSbzBEXzMOb_ewW3xNO1jTodBbqBHD9AKqD_sF1kp_xLqn17DiSaB3UBDYvSYvRj8XePO0npLvV5d355-bm6_XX87Pbpoge14b3yvORN8PndICmLZbpa1Uwdh-VNzoQQ-jGYH3vZQCR8zzsPUqjEJrCFLJU_Lh2Huf088D3u2WWALMs18Bn-uExD5rhWGIvv8HndIh41-Q6rpOWS2FRIofqZBTKRlGd5_j4vOD48w9-neTQ__u0b9jwqF_zLx7aj5sFxj-Jv4IR-DTEQBU8StCdiVEWANKzhCqG1L8T_1vcVqUkQ</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Chen, Chonglin</creator><creator>Huang, Sijian</creator><creator>Sun, Limei</creator><creator>Li, Songshan</creator><creator>Huang, Li</creator><creator>Wang, Zhirong</creator><creator>Luo, Xiaoling</creator><creator>Ding, Xiaoyan</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20201001</creationdate><title>Analysis of Etiologic Factors in Pediatric Rhegmatogenous Retinal Detachment With Genetic Testing</title><author>Chen, Chonglin ; Huang, Sijian ; Sun, Limei ; Li, Songshan ; Huang, Li ; Wang, Zhirong ; Luo, Xiaoling ; Ding, Xiaoyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-a8510288d4562e069b56935c798f5176d6df7fe1883328f50a1cba5cf266ec353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Age</topic><topic>Cataracts</topic><topic>Congenital diseases</topic><topic>Disease</topic><topic>Etiology</topic><topic>Families & family life</topic><topic>Genetic testing</topic><topic>Marfan syndrome</topic><topic>Mutation</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Retina</topic><topic>Retinal detachment</topic><topic>Risk factors</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Chonglin</creatorcontrib><creatorcontrib>Huang, Sijian</creatorcontrib><creatorcontrib>Sun, Limei</creatorcontrib><creatorcontrib>Li, Songshan</creatorcontrib><creatorcontrib>Huang, Li</creatorcontrib><creatorcontrib>Wang, Zhirong</creatorcontrib><creatorcontrib>Luo, Xiaoling</creatorcontrib><creatorcontrib>Ding, Xiaoyan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Chonglin</au><au>Huang, Sijian</au><au>Sun, Limei</au><au>Li, Songshan</au><au>Huang, Li</au><au>Wang, Zhirong</au><au>Luo, Xiaoling</au><au>Ding, Xiaoyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Etiologic Factors in Pediatric Rhegmatogenous Retinal Detachment With Genetic Testing</atitle><jtitle>American journal of ophthalmology</jtitle><addtitle>Am J Ophthalmol</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>218</volume><spage>330</spage><epage>336</epage><pages>330-336</pages><issn>0002-9394</issn><eissn>1879-1891</eissn><abstract>The purpose of this study was to investigate the etiology and clinical features of nontraumatic rhegmatogenous retinal detachment (RRD) in children.
Consecutive, cross-sectional study.
In this study, 112 operative eyes of 102 patients ≤18 years of age with nontraumatic RRD were included. Comprehensive ophthalmic examinations were performed in all patients. Genetic testing was performed in 34 patients with hereditary congenital/developmental diseases. The etiology of RRD was analyzed.
The average age was 12.2 ± 4.5 years (range, 1-18 years). The percentages of male and female patients were 74.5% (76/102) and 25.5% (26/102), respectively. The most common etiologic factors were congenital/developmental anomalies (51/102, 50%), followed by simple myopia (34/102, 33.3%) and previous intraocular surgery (6/102, 5.9%). More than half (31/51, 60.8%) of the patients with congenital/developmental anomalies had familial exudative vitreoretinopathy. Further analysis of the underlying etiologic factors based on age revealed that the most common etiology of RRD in patients ≤12 years of age was congenital/developmental anomalies (28/48, 58.3%); however, simple myopia was the major etiologic factor in patients >12 years of age (27/54, 50%).
Congenital/developmental diseases were the most common etiologies of pediatric nontraumatic RRD in China. Familial exudative vitreoretinopathy accounted for most of the congenital/developmental anomalies.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32112773</pmid><doi>10.1016/j.ajo.2020.02.015</doi><tpages>7</tpages></addata></record> |
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subjects | Age Cataracts Congenital diseases Disease Etiology Families & family life Genetic testing Marfan syndrome Mutation Patients Pediatrics Retina Retinal detachment Risk factors Surgery |
title | Analysis of Etiologic Factors in Pediatric Rhegmatogenous Retinal Detachment With Genetic Testing |
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