Villegas Victor M, Chang Jonathan S, Hess Ditte J, Berrocal Audina M
Bascom Palmer Eye Institute, Jackson Memorial Hospital, University of Miami Miller School of Medicine, Miami, FL, USA.
J Pediatr Ophthalmol Strabismus. 2013 Jun 4;50 Online:e24-6. doi: 10.3928/01913913-20130528-02.
The authors report the first case of trisomy 18 associated with a clinically detectable optic nerve pit. A female infant with a birth weight of 2,150 g was born by cesarean section to a healthy 40-year-old woman at 38 weeks of gestation. Trisomy 18 had been diagnosed by prenatal genetic testing. Ophthalmologic examination was remarkable for bilateral narrowed palpebral fissures with punctal agenesis, corectopic pupils without reaction to light, bilateral inferior peripapillary retinochoroidal hypopigmentation, and significant optic nerve cupping in the left eye with associated temporal optic nerve pit. It has generally been accepted that optic nerve pits are a congenital anomaly. However, the pathophysiological background of optic nerve pits remains unclear and controversial. This is the first clinical and photographic documentation of an optic nerve pit in a neonate and in Edwards syndrome.
作者报告了首例18三体综合征合并临床可检测到的视神经凹陷病例。一名出生体重2150克的女婴在妊娠38周时由剖宫产出生,其母亲是一名健康的40岁女性。产前基因检测诊断为18三体综合征。眼科检查发现显著异常,包括双侧睑裂狭窄伴泪点缺如、瞳孔异位且对光无反应、双侧视乳头周围视网膜脉络膜色素减退,以及左眼明显的视神经杯状凹陷并伴有颞侧视神经凹陷。一般认为视神经凹陷是一种先天性异常。然而,视神经凹陷的病理生理背景仍不清楚且存在争议。这是新生儿及爱德华兹综合征中视神经凹陷的首例临床及影像学记录。