显性遗传性上睑下垂、高度近视和晶状体异位。
Dominantly inherited blepharoptosis, high myopia, and ectopia lentis.
作者信息
Gillum W N, Anderson R L
出版信息
Arch Ophthalmol. 1982 Feb;100(2):282-4. doi: 10.1001/archopht.1982.01030030284010.
Abstract
A previously undescribed syndrome of bilateral blepharoptosis, ectopia lentis, and high myopia apparently was dominantly inherited and originated from a spontaneous genetic mutation. The syndrome seems to be caused by a decrease in the tensile strength of the levator aponeurosis, the zonules, and the sclera.
摘要
一种先前未被描述的双侧上睑下垂、晶状体异位和高度近视综合征显然是显性遗传的，且源于自发基因突变。该综合征似乎是由提上睑肌腱膜、晶状体悬韧带和巩膜的抗张强度降低所致。
Zotero 插件