The Vision Center at Children's Hospital Los Angeles, 4650 Sunset Blvd. MS#88, Los Angeles, CA, 90027, USA,
Curr Treat Options Neurol. 2013 Feb;15(1):78-89. doi: 10.1007/s11940-012-0209-2.
Optic nerve hypoplasia (ONH) has developed into a leading cause of congenital blindness. The frequently associated features of hypopituitarism and absent septum pellucidum were felt to have embryonic linkage as "septo-optic dysplasia" or "de Morsier's syndrome." More recent studies have suggested these associations are independent of one another. This review provides an assessment of the historical and recent evidence linking neuroradiologic, endocrinologic and developmental morbidity in patients with ONH. The prenatal risk factors, heritability, and genetic mutations associated with ONH are described.
Recognition of the critical association of ONH with hypopituitarism should be attributed to William Hoyt, not Georges de Morsier. De Morsier never described a case of ONH or recognized its association with hypopituitarism or missing septum pellucidum. Hypopituitarism is caused by hypothalamic dysfunction. This, and other more recently identified associations with ONH, such as developmental delay and autism, are independent of septum pellucidum development. Other common neuroradiographic associations such as corpus callosum hypoplasia, gyrus dysplasia, and cortical heterotopia may have prognostic significance. The predominant prenatal risk factors for ONH are primiparity and young maternal age. Presumed risk factors such as prenatal exposure to drugs and alcohol are not supported by scrutiny of the literature. Heritability and identified gene mutations in cases of ONH are rare.
Children with ONH require monitoring for many systemic, developmental, and even life-threatening problems independent of the severity of ONH and presence of brain malformations including abnormalities of the septum pellucidum. "Septo-optic dysplasia" and "de Morsier's syndrome" are historically inaccurate and clinically misleading terms.
视神经发育不全(ONH)已成为先天性失明的主要原因。常伴有垂体功能减退和透明隔缺失的特征,被认为具有胚胎关联性,称为“视隔发育不良”或“德莫尔西耶综合征”。最近的研究表明,这些关联彼此独立。本综述评估了将视神经发育不全患者的神经放射学、内分泌和发育发病率联系起来的历史和近期证据。描述了与 ONH 相关的产前危险因素、遗传性和基因突变。
应将视神经发育不全与垂体功能减退的重要关联性归因于 William Hoyt,而不是 Georges de Morsier。德莫尔西耶从未描述过视神经发育不全的病例,也没有认识到其与垂体功能减退或透明隔缺失有关。垂体功能减退是由下丘脑功能障碍引起的。这种情况,以及最近其他与视神经发育不全相关的情况,如发育迟缓与自闭症,与透明隔的发育无关。其他常见的神经影像学关联,如胼胝体发育不全、脑回发育不良和皮质异位,可能具有预后意义。视神经发育不全的主要产前危险因素是初产妇和年轻产妇。普遍认为的产前危险因素,如暴露于药物和酒精,并没有得到文献审查的支持。视神经发育不全病例中的遗传性和已确定的基因突变罕见。
视神经发育不全的儿童需要监测许多系统性、发育性甚至危及生命的问题,而与视神经发育不全的严重程度以及包括透明隔异常在内的脑畸形无关。“视隔发育不良”和“德莫尔西耶综合征”在历史上不准确,临床上具有误导性。