Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: a review of 141 cases
Aims: To determine the visual outcome and prevalence of amblyogenic risk factors in children with craniosynostotic syndromes. Methods: The case notes of 141 children seen within the craniofacial unit were reviewed and information retrieved on date of birth, age at first and last examination, cyclopl...
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Veröffentlicht in: | British journal of ophthalmology 2003-08, Vol.87 (8), p.999-1003 |
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description | Aims: To determine the visual outcome and prevalence of amblyogenic risk factors in children with craniosynostotic syndromes. Methods: The case notes of 141 children seen within the craniofacial unit were reviewed and information retrieved on date of birth, age at first and last examination, cycloplegic refraction at last visit, best corrected visual acuity at last visit, horizontal ocular deviation in primary position at first visit, and alphabet pattern if any. The presence of astigmatism, its magnitude, and orientation of axis were determined. Results: 40.3% of patients had 1 dioptre (D) of astigmatism or greater and, of these, 64% had oblique astigmatism in at least one eye. Anisometropia of 1D or more was found in 18% of patients (age matched normals 3.5%). Horizontal strabismus was found in 70% (38% exotropia, 32% esotropia). Visual outcome results showed 39.8% of patients (45 of 113) had visual acuity of 6/12 or worse in their better eye. Conclusion: In the largest study to date a poor visual outcome was shown in children with Crouzon’s, Pfeiffer’s, Apert’s, and Saethre-Chotzen syndromes (39.8% with 6/12 or worse in the better eye) together with significant prevalence of amblyogenic risk factors. |
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Methods: The case notes of 141 children seen within the craniofacial unit were reviewed and information retrieved on date of birth, age at first and last examination, cycloplegic refraction at last visit, best corrected visual acuity at last visit, horizontal ocular deviation in primary position at first visit, and alphabet pattern if any. The presence of astigmatism, its magnitude, and orientation of axis were determined. Results: 40.3% of patients had 1 dioptre (D) of astigmatism or greater and, of these, 64% had oblique astigmatism in at least one eye. Anisometropia of 1D or more was found in 18% of patients (age matched normals 3.5%). Horizontal strabismus was found in 70% (38% exotropia, 32% esotropia). Visual outcome results showed 39.8% of patients (45 of 113) had visual acuity of 6/12 or worse in their better eye. Conclusion: In the largest study to date a poor visual outcome was shown in children with Crouzon’s, Pfeiffer’s, Apert’s, and Saethre-Chotzen syndromes (39.8% with 6/12 or worse in the better eye) together with significant prevalence of amblyogenic risk factors.</description><identifier>ISSN: 0007-1161</identifier><identifier>EISSN: 1468-2079</identifier><identifier>DOI: 10.1136/bjo.87.8.999</identifier><identifier>PMID: 12881344</identifier><identifier>CODEN: BJOPAL</identifier><language>eng</language><publisher>BMA House, Tavistock Square, London, WC1H 9JR: BMJ Publishing Group Ltd</publisher><subject>Adolescent ; Age ; amblyopia ; Amblyopia - etiology ; Astigmatism ; Astigmatism - etiology ; Biological and medical sciences ; Births ; Child ; Child, Preschool ; children ; Clinical Science - Extended Reports ; Craniosynostoses - complications ; Craniosynostoses - physiopathology ; craniosynostosis ; Craniotomy ; Diseases of the osteoarticular system ; Humans ; Infant ; Malformations and congenital and or hereditary diseases involving bones. Joint deformations ; Medical sciences ; Prognosis ; Retrospective Studies ; Risk Factors ; Strabismus - etiology ; Syndrome ; Vision Disorders - etiology ; Visual Acuity</subject><ispartof>British journal of ophthalmology, 2003-08, Vol.87 (8), p.999-1003</ispartof><rights>Copyright 2003 British Journal of Ophthalmology</rights><rights>2003 INIST-CNRS</rights><rights>COPYRIGHT 2003 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2003 Copyright 2003 British Journal of Ophthalmology</rights><rights>Copyright © Copyright 2003 British Journal of Ophthalmology 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b585t-b42b8e9db355ed5159a0f585c1fff8726b61df40fb643b374fee2927ac00e6263</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1771801/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1771801/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14980204$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12881344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khan, S H</creatorcontrib><creatorcontrib>Nischal, K K</creatorcontrib><creatorcontrib>Dean, F</creatorcontrib><creatorcontrib>Hayward, R D</creatorcontrib><creatorcontrib>Walker, J</creatorcontrib><title>Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: a review of 141 cases</title><title>British journal of ophthalmology</title><addtitle>Br J Ophthalmol</addtitle><description>Aims: To determine the visual outcome and prevalence of amblyogenic risk factors in children with craniosynostotic syndromes. Methods: The case notes of 141 children seen within the craniofacial unit were reviewed and information retrieved on date of birth, age at first and last examination, cycloplegic refraction at last visit, best corrected visual acuity at last visit, horizontal ocular deviation in primary position at first visit, and alphabet pattern if any. The presence of astigmatism, its magnitude, and orientation of axis were determined. Results: 40.3% of patients had 1 dioptre (D) of astigmatism or greater and, of these, 64% had oblique astigmatism in at least one eye. Anisometropia of 1D or more was found in 18% of patients (age matched normals 3.5%). Horizontal strabismus was found in 70% (38% exotropia, 32% esotropia). Visual outcome results showed 39.8% of patients (45 of 113) had visual acuity of 6/12 or worse in their better eye. Conclusion: In the largest study to date a poor visual outcome was shown in children with Crouzon’s, Pfeiffer’s, Apert’s, and Saethre-Chotzen syndromes (39.8% with 6/12 or worse in the better eye) together with significant prevalence of amblyogenic risk factors.</description><subject>Adolescent</subject><subject>Age</subject><subject>amblyopia</subject><subject>Amblyopia - etiology</subject><subject>Astigmatism</subject><subject>Astigmatism - etiology</subject><subject>Biological and medical sciences</subject><subject>Births</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>children</subject><subject>Clinical Science - Extended Reports</subject><subject>Craniosynostoses - complications</subject><subject>Craniosynostoses - physiopathology</subject><subject>craniosynostosis</subject><subject>Craniotomy</subject><subject>Diseases of the osteoarticular system</subject><subject>Humans</subject><subject>Infant</subject><subject>Malformations and congenital and or hereditary diseases involving bones. Joint deformations</subject><subject>Medical sciences</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Strabismus - etiology</subject><subject>Syndrome</subject><subject>Vision Disorders - etiology</subject><subject>Visual Acuity</subject><issn>0007-1161</issn><issn>1468-2079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9ks9vFCEUxydGY7fVm2dDYtSLswIzA4wHk2ajrclGY6J7JcA8VrYz0MJM6_73stlNW01jOPDjfd738eBbFC8InhNSsfd6E-aCz8W8bdtHxYzUTJQU8_ZxMcMY85IQRo6K45Q2eUsZ4U-LI0KFIFVdzwq1cmlSPQrTaMIACSnfITXofhvW4J1B0aULZJUZQ0zIeWSi8i6krQ9pDGMG8rKLu9QPSKEI1w5uULCI1AQZlSA9K55Y1Sd4fphPip-fP_1YnJfLb2dfFqfLUjeiGUtdUy2g7XTVNNA1pGkVtjliiLVWcMo0I52tsdWsrnTFawtAW8qVwRgYZdVJ8XGveznpAToDfoyql5fRDSpuZVBO_h3x7pdch2tJOCcCkyzw5iAQw9UEaZSDSwb6XnkIU5K8ajDlWGTw1T_gJkzR5-Z2Wi3GLavqTJV7aq16kM7bkKua_KiQiwcP1uXjU4KZYDgrZ37-AJ9HB4MzDya82yeYGFKKYG97JVjurCGzNaTgUshsjYy_vP8-d_DBCxl4fQBUMqq3-aONS3dc3QpM8b3GXBrh921cxQvJeMUb-XW1kGd0dc6X35eyyfzbPa-Hzf-v-AeJYN20</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Khan, S H</creator><creator>Nischal, K K</creator><creator>Dean, F</creator><creator>Hayward, R D</creator><creator>Walker, J</creator><general>BMJ Publishing Group Ltd</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><general>Copyright 2003 British Journal of Ophthalmology</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030801</creationdate><title>Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: a review of 141 cases</title><author>Khan, S H ; Nischal, K K ; Dean, F ; Hayward, R D ; Walker, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b585t-b42b8e9db355ed5159a0f585c1fff8726b61df40fb643b374fee2927ac00e6263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adolescent</topic><topic>Age</topic><topic>amblyopia</topic><topic>Amblyopia - etiology</topic><topic>Astigmatism</topic><topic>Astigmatism - etiology</topic><topic>Biological and medical sciences</topic><topic>Births</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>children</topic><topic>Clinical Science - Extended Reports</topic><topic>Craniosynostoses - complications</topic><topic>Craniosynostoses - physiopathology</topic><topic>craniosynostosis</topic><topic>Craniotomy</topic><topic>Diseases of the osteoarticular system</topic><topic>Humans</topic><topic>Infant</topic><topic>Malformations and congenital and or hereditary diseases involving bones. Joint deformations</topic><topic>Medical sciences</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Strabismus - etiology</topic><topic>Syndrome</topic><topic>Vision Disorders - etiology</topic><topic>Visual Acuity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khan, S H</creatorcontrib><creatorcontrib>Nischal, K K</creatorcontrib><creatorcontrib>Dean, F</creatorcontrib><creatorcontrib>Hayward, R D</creatorcontrib><creatorcontrib>Walker, J</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of ophthalmology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khan, S H</au><au>Nischal, K K</au><au>Dean, F</au><au>Hayward, R D</au><au>Walker, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: a review of 141 cases</atitle><jtitle>British journal of ophthalmology</jtitle><addtitle>Br J Ophthalmol</addtitle><date>2003-08-01</date><risdate>2003</risdate><volume>87</volume><issue>8</issue><spage>999</spage><epage>1003</epage><pages>999-1003</pages><issn>0007-1161</issn><eissn>1468-2079</eissn><coden>BJOPAL</coden><abstract>Aims: To determine the visual outcome and prevalence of amblyogenic risk factors in children with craniosynostotic syndromes. Methods: The case notes of 141 children seen within the craniofacial unit were reviewed and information retrieved on date of birth, age at first and last examination, cycloplegic refraction at last visit, best corrected visual acuity at last visit, horizontal ocular deviation in primary position at first visit, and alphabet pattern if any. The presence of astigmatism, its magnitude, and orientation of axis were determined. Results: 40.3% of patients had 1 dioptre (D) of astigmatism or greater and, of these, 64% had oblique astigmatism in at least one eye. Anisometropia of 1D or more was found in 18% of patients (age matched normals 3.5%). Horizontal strabismus was found in 70% (38% exotropia, 32% esotropia). Visual outcome results showed 39.8% of patients (45 of 113) had visual acuity of 6/12 or worse in their better eye. Conclusion: In the largest study to date a poor visual outcome was shown in children with Crouzon’s, Pfeiffer’s, Apert’s, and Saethre-Chotzen syndromes (39.8% with 6/12 or worse in the better eye) together with significant prevalence of amblyogenic risk factors.</abstract><cop>BMA House, Tavistock Square, London, WC1H 9JR</cop><pub>BMJ Publishing Group Ltd</pub><pmid>12881344</pmid><doi>10.1136/bjo.87.8.999</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Age amblyopia Amblyopia - etiology Astigmatism Astigmatism - etiology Biological and medical sciences Births Child Child, Preschool children Clinical Science - Extended Reports Craniosynostoses - complications Craniosynostoses - physiopathology craniosynostosis Craniotomy Diseases of the osteoarticular system Humans Infant Malformations and congenital and or hereditary diseases involving bones. Joint deformations Medical sciences Prognosis Retrospective Studies Risk Factors Strabismus - etiology Syndrome Vision Disorders - etiology Visual Acuity |
title | Visual outcomes and amblyogenic risk factors in craniosynostotic syndromes: a review of 141 cases |
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