Angioid streaks in a case of Camurati–Engelmann disease
Camurati–Engelmann disease (CED) is a rare autosomal dominant disease with various phenotypic expressions. The hallmark of the disease is bilateral symmetric diaphyseal hyperostosis of the long bones with progressive involvement of the metaphysis. Ocular manifestations occur rarely and mainly result...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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Wolters Kluwer Medknow Publications
2017-01-01
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| Series: | Indian Journal of Ophthalmology |
| Subjects: | |
| Online Access: | http://www.ijo.in/article.asp?issn=0301-4738;year=2017;volume=65;issue=7;spage=628;epage=630;aulast=Tugcu |
| _version_ | 1831753542907461632 |
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| author | Betül Tugcu Taha Sezer Ahmet Elbay Hakan Özdemir |
| author_facet | Betül Tugcu Taha Sezer Ahmet Elbay Hakan Özdemir |
| author_sort | Betül Tugcu |
| collection | DOAJ |
| description | Camurati–Engelmann disease (CED) is a rare autosomal dominant disease with various phenotypic expressions. The hallmark of the disease is bilateral symmetric diaphyseal hyperostosis of the long bones with progressive involvement of the metaphysis. Ocular manifestations occur rarely and mainly result from bony overgrowth of the orbit and optic canal stenosis. We report a case of CED showing angioid streaks (ASs) in both fundi with no macular involvement and discuss the possible theories of the pathogenesis of AS in this disease. |
| first_indexed | 2024-12-21T23:22:37Z |
| format | Article |
| id | doaj.art-20738eeab1a247f3ba668d18484853f3 |
| institution | Directory Open Access Journal |
| issn | 0301-4738 1998-3689 |
| language | English |
| last_indexed | 2024-12-21T23:22:37Z |
| publishDate | 2017-01-01 |
| publisher | Wolters Kluwer Medknow Publications |
| record_format | Article |
| series | Indian Journal of Ophthalmology |
| spelling | doaj.art-20738eeab1a247f3ba668d18484853f32022-12-21T18:46:44ZengWolters Kluwer Medknow PublicationsIndian Journal of Ophthalmology0301-47381998-36892017-01-0165762863010.4103/ijo.IJO_910_16Angioid streaks in a case of Camurati–Engelmann diseaseBetül TugcuTaha SezerAhmet ElbayHakan ÖzdemirCamurati–Engelmann disease (CED) is a rare autosomal dominant disease with various phenotypic expressions. The hallmark of the disease is bilateral symmetric diaphyseal hyperostosis of the long bones with progressive involvement of the metaphysis. Ocular manifestations occur rarely and mainly result from bony overgrowth of the orbit and optic canal stenosis. We report a case of CED showing angioid streaks (ASs) in both fundi with no macular involvement and discuss the possible theories of the pathogenesis of AS in this disease.http://www.ijo.in/article.asp?issn=0301-4738;year=2017;volume=65;issue=7;spage=628;epage=630;aulast=TugcuAngioid streakCamurati–Engelmann diseaseconnective tissue disorderretina |
| spellingShingle | Betül Tugcu Taha Sezer Ahmet Elbay Hakan Özdemir Angioid streaks in a case of Camurati–Engelmann disease Indian Journal of Ophthalmology Angioid streak Camurati–Engelmann disease connective tissue disorder retina |
| title | Angioid streaks in a case of Camurati–Engelmann disease |
| title_full | Angioid streaks in a case of Camurati–Engelmann disease |
| title_fullStr | Angioid streaks in a case of Camurati–Engelmann disease |
| title_full_unstemmed | Angioid streaks in a case of Camurati–Engelmann disease |
| title_short | Angioid streaks in a case of Camurati–Engelmann disease |
| title_sort | angioid streaks in a case of camurati engelmann disease |
| topic | Angioid streak Camurati–Engelmann disease connective tissue disorder retina |
| url | http://www.ijo.in/article.asp?issn=0301-4738;year=2017;volume=65;issue=7;spage=628;epage=630;aulast=Tugcu |
| work_keys_str_mv | AT betultugcu angioidstreaksinacaseofcamuratiengelmanndisease AT tahasezer angioidstreaksinacaseofcamuratiengelmanndisease AT ahmetelbay angioidstreaksinacaseofcamuratiengelmanndisease AT hakanozdemir angioidstreaksinacaseofcamuratiengelmanndisease |