{"created":"2023-07-27T06:29:01.000406+00:00","id":13659,"links":{},"metadata":{"_buckets":{"deposit":"735e3020-3c58-4846-a49c-02d4503204ca"},"_deposit":{"created_by":3,"id":"13659","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"13659"},"status":"published"},"_oai":{"id":"oai:kanazawa-u.repo.nii.ac.jp:00013659","sets":["1132:1133:1134"]},"author_link":["22694","22695","880","22809"],"item_4_biblio_info_8":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2009-06-10","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"6","bibliographicPageEnd":"671","bibliographicPageStart":"664","bibliographicVolumeNumber":"113","bibliographic_titles":[{"bibliographic_title":"日本眼科學会雜誌 = Journal of Japanese Ophthalmological Society"}]}]},"item_4_description_21":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"目的：家族内発生と考えられたsuperior segmental optic hypoplasia(以下SSOH)を含む視神経低形成の2家系について報告する. 症例：症例1(家系1)と症例2(家系1)は姉妹例である. 症例3(家系2)と症例4(家系2)は親子例, 症例3と症例5(家系2)は兄妹例である. 家系1の2症例はそれぞれ片眼のSSOHであったが, 家系2の3症例は同一家系内でもSSOH, 視神経鼻側低形成, 広範囲な視神経低形成と多様な病像を呈した. 症例1と3は前医で正常眼圧緑内障と診断され, 点眼加療されていた. 今回示した症例の中では全身疾患を有するものはない. 症例1と2, 症例3と5の父は2型糖尿病で治療中であった. 結論：視神経低形成は家族内発生することがある. また家系2の3症例から, 同一家系内でも視神経の低形成は上方のものから, 鼻側, 広範囲な低形成まで多彩であり, SSOHは視神経低形成の一亜型と考えられた. 　　Purpose : To report two familial cases of optic nerve hypoplasia including superior segmental optic hypoplasia (SSOH). Cases : In Family 1, case 1 and case 2 were sisters. In Family 2, case 3 was the mother of case 4 and the younger sister of case 5. The cases in Family 1 had SSOH in one eye, whereas Family 2 showed various patterns of SSOH, as well as nasal optic nerve hypoplasia, and a wide range of optic nerve hypoplasia. Case 1 and case 3 were diagnosed as normal tension glaucoma and treated with eye drops at a previous hospital. None of the cases had any systemic illness. The father of cases 1 and 2, and the father of Cases 3 and 5 were under treatment for type 2 diabetes mellitus. Conclusion : In this study, SSOH seemed to be prevalent among family members. In addition, as the cases in Family 2 illustrate, hypoplasia of the optic nerve showed various patterns in the superior segment, nasal segment, and over a wide range of the optic nerve. Therefore SSOH was just one part of the overall optic nerve hypoplasia.","subitem_description_type":"Abstract"}]},"item_4_publisher_17":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"日本眼科学会 = Japanese Ophthalmological Society"}]},"item_4_relation_28":{"attribute_name":"関連URI","attribute_value_mlt":[{"subitem_relation_type_id":{"subitem_relation_type_id_text":"http://www.nichigan.or.jp/member/journal/nggz/index.jsp","subitem_relation_type_select":"URI"}},{"subitem_relation_type_id":{"subitem_relation_type_id_text":"http://ci.nii.ac.jp/naid/10025148470/","subitem_relation_type_select":"URI"}}]},"item_4_rights_23":{"attribute_name":"権利","attribute_value_mlt":[{"subitem_rights":"Copyright © Japanese Ophthalmological Society"}]},"item_4_rights_24":{"attribute_name":"権利URI","attribute_value_mlt":[{"subitem_rights":"http://www.nichigan.or.jp/index.jsp"}]},"item_4_source_id_11":{"attribute_name":"NCID","attribute_value_mlt":[{"subitem_source_identifier":"AN00187157","subitem_source_identifier_type":"NCID"}]},"item_4_source_id_9":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0029-0203","subitem_source_identifier_type":"ISSN"}]},"item_4_version_type_25":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"高田, 祥平"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"新田, 耕治"}],"nameIdentifiers":[{},{},{}]},{"creatorNames":[{"creatorName":"棚橋, 俊郎"}],"nameIdentifiers":[{},{}]},{"creatorNames":[{"creatorName":"杉山, 和久"}],"nameIdentifiers":[{},{},{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2017-10-03"}],"displaytype":"detail","filename":"ME-PR-SUGIYAMA-K-664.pdf","filesize":[{"value":"4.9 MB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"ME-PR-SUGIYAMA-K-664.pdf","url":"https://kanazawa-u.repo.nii.ac.jp/record/13659/files/ME-PR-SUGIYAMA-K-664.pdf"},"version_id":"db96191a-c866-4480-af03-4bcfb34c6ae4"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"jpn"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"Superior segmental optic hypoplasia を含む視神経低形成の2家系","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Superior segmental optic hypoplasia を含む視神経低形成の2家系"},{"subitem_title":"Two Familial Cases of Optic Nerve Hypoplasia Including Superior Segmental Optic Hypoplasia","subitem_title_language":"en"}]},"item_type_id":"4","owner":"3","path":["1134"],"pubdate":{"attribute_name":"公開日","attribute_value":"2017-10-03"},"publish_date":"2017-10-03","publish_status":"0","recid":"13659","relation_version_is_last":true,"title":["Superior segmental optic hypoplasia を含む視神経低形成の2家系"],"weko_creator_id":"3","weko_shared_id":-1},"updated":"2023-07-28T01:00:45.336134+00:00"}