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pubmed-article:19951599pubmed:abstractTextBlepharophimosis ptosis epicanthus inversus syndrome (BPES) is a rare congenital ophthalmic disorder, characterized by congenital eyelid malformation including bilateral ptosis, shortening of the horizontal eyelid fissure, epicanthus inversus, and increased distance between the inner canthi. In this research, we studied the histological structure and ultrastructure of medial canthal ligament of patients with BPES.lld:pubmed
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pubmed-article:19951599pubmed:monthNovlld:pubmed
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pubmed-article:19951599pubmed:authorpubmed-author:GeJianJlld:pubmed
pubmed-article:19951599pubmed:authorpubmed-author:FONTA JAJlld:pubmed
pubmed-article:19951599pubmed:authorpubmed-author:ZhongXiu-feng...lld:pubmed
pubmed-article:19951599pubmed:authorpubmed-author:HuangDan-ping...lld:pubmed
pubmed-article:19951599pubmed:authorpubmed-author:ZhuoYe-hongYHlld:pubmed
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pubmed-article:19951599pubmed:authorpubmed-author:YuYang-yangYYlld:pubmed
pubmed-article:19951599pubmed:authorpubmed-author:LaiZhao-guang...lld:pubmed
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pubmed-article:19951599pubmed:year2009lld:pubmed
pubmed-article:19951599pubmed:articleTitleHistological and ultrastructural study on the medial canthal ligament of blepharophimosis, ptosis and epicanthus inversus syndrome.lld:pubmed
pubmed-article:19951599pubmed:affiliationDepartment of Plastic Surgery, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.lld:pubmed
pubmed-article:19951599pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19951599pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed