Mathys R, Deconinck H, Keymolen K, Jansen A, Van Esch H
Department of Paediatric Ophthalmology, UZ Brussel, Brussels, Belgium.
Bull Soc Belge Ophtalmol. 2007(305):49-53.
We present the ophthalmologic findings in a boy with a deletion of Xp22 comprising the gene for Nance-Horan syndrome. Different mechanisms underlying the visual impairment in Nance-Horan syndrome are discussed.
我们报告了一名患有Xp22缺失（包含南斯-霍兰综合征基因）男孩的眼科检查结果。本文讨论了南斯-霍兰综合征视力损害的不同潜在机制。
