Association of type II Waardenburg syndrome with hypermetropic amblyopia.
作者信息
Chua Shee Wen, Mohd Khialdin Safinaz, Mustapha Mushawiahti, Md Din Norshamsiah, Yong Meng Hsien
机构信息
Department of Ophthalmology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur 56000, Malaysia.
Ophthalmology Department, Faculty of Medicine and Health Sciences, Universiti Malaysia Sabah, Kota Kinabalu 88400, Sabah, Malaysia.
出版信息
Int J Ophthalmol. 2022 Apr 18;15(4):677-680. doi: 10.18240/ijo.2022.04.26. eCollection 2022.
Abstract
摘要
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注：原文中“civilian life”直译为“平民生活”，结合语境这里可意译为“日常生活”等更合适的表述，但按要求不添加其他解释或说明，保留原文英文表述。
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Whole genome genotyping mapped regions on chromosome 2 and 18 in a family segregating Waardenburg syndrome type II.对一个患有Ⅱ型瓦登伯革氏综合征的家系进行全基因组基因分型，确定了2号和18号染色体上的定位区域。
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Anisometropic amblyopia in a case of type 2 Waardenburg syndrome.2型瓦尔登堡综合征病例中的屈光参差性弱视。
BMJ Case Rep. 2013 Dec 18;2013:bcr2013201140. doi: 10.1136/bcr-2013-201140.
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Ophthalmological screening of a paediatric cochlear implant population: a retrospective analysis and 12-year follow-up.小儿人工耳蜗植入人群的眼科筛查：回顾性分析和 12 年随访。
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Waardenburg syndrome.瓦登伯革氏综合征
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