Leitch R J, Winter R M
Institute of Child Health, London, UK.
Acta Ophthalmol Scand Suppl. 1996(219):16-9. doi: 10.1111/j.1600-0420.1996.tb00375.x.
A case with a severe midline craniofacial defect, comprising a midline cleft lip and palate with a sphenoethmoidal encephalocele, hypertelorism, bilateral dysplastic optic discs and agenesis of the corpus callosum is described. The optic discs are consistent with the spectrum of appearances seen in the Morning Glory Disc Anomaly (MGDA). This anomaly is usually a uniocular problem that may be rarely associated with craniofacial abnormalities. Despite this range of abnormalities this child was developing well with a specific motor delay at the age of eight months. Cases with similar midline craniofacial abnormalities from the literature are reviewed. This condition appears to be a distinct entity within the spectrum of frontonasal dysplasia.
本文描述了一例严重的中线颅面缺损病例,包括中线唇腭裂伴蝶筛部脑膨出、眼距过宽、双侧视神经盘发育异常和胼胝体发育不全。视神经盘与牵牛花综合征(MGDA)所见的一系列表现相符。这种异常通常是单眼问题,很少与颅面异常相关。尽管存在一系列异常情况,但该患儿在8个月大时发育良好,有特定的运动发育迟缓。本文回顾了文献中具有类似中线颅面异常的病例。这种情况似乎是额鼻发育异常谱系中的一个独特实体。