Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Ophthalmology, Greenlane Clinical Centre, Te Whatu Ora - Health New Zealand, Auckland, New Zealand.
J Paediatr Child Health. 2024 Oct;60(10):516-525. doi: 10.1111/jpc.16624. Epub 2024 Jul 25.
Hypovitaminosis A is a leading cause of preventable childhood blindness, especially in developing nations. Vitamin A is a fat-soluble essential micronutrient that serves vital functions in the visual system and in regulating bone resorption. We report on a series of four children with mixed nutritional and compressive optic neuropathy and provide a review of the literature.
A retrospective observational study of four males (ages 9-12), three with autism spectrum disorder who presented with loss of vision and multiple vitamin deficiencies including hypovitaminosis A.
Patients presented with unexplained visual loss or a change in visual behaviour. All patients had severely restricted diet comprising of predominantly carbohydrates. Two of the four cases demonstrated optic nerve pallor at initial presentation with marked optic atrophy developing in all patients over time. Electrophysiology available in two patients demonstrated optic nerve dysfunction with preserved retinal function. Extensive investigations revealed profound deficiency in multiple vitamins including vitamin A (<0.1-0.2 μmol/L, normal = 0.9-1.7 μmol/L). Three patients also had low vitamin B12 (90-111 pmol/L, normal = 170-800 pmol/L) with normal folate. All four cases had radiological evidence of skull base thickening indicative of low vitamin A. Genetic testing did not find any relevant pathogenic variants.
Hypovitaminosis A is a crucial form of nutritional deprivation that results in significant visual loss with potential hyperostosis and optic nerve compression exacerbating nutritional optic neuropathy. Additional micronutrient deficiencies usually co-exist and may contribute. Extra vigilance in vitamin replacement is required of clinicians with patients with autism who have restricted diets.
维生素 A 缺乏是可预防的儿童失明的主要原因,尤其是在发展中国家。维生素 A 是一种脂溶性必需微量营养素,在视觉系统和调节骨吸收中发挥重要作用。我们报告了一系列 4 例伴有混合性营养性和压迫性视神经病变的儿童病例,并对文献进行了回顾。
对 4 名男性(年龄 9-12 岁)进行回顾性观察性研究,其中 3 名患有自闭症谱系障碍,他们因视力丧失和多种维生素缺乏(包括维生素 A 缺乏)而就诊。
患者表现为原因不明的视力丧失或视觉行为改变。所有患者的饮食都受到严重限制,主要由碳水化合物组成。其中 4 例中有 2 例在初始表现时视神经苍白,所有患者随时间推移均出现明显的视神经萎缩。在 2 例患者中可进行电生理检查,结果显示视神经功能障碍,视网膜功能正常。广泛的检查显示多种维生素严重缺乏,包括维生素 A(<0.1-0.2μmol/L,正常范围为 0.9-1.7μmol/L)。3 例患者还存在维生素 B12 水平低(90-111pmol/L,正常范围为 170-800pmol/L),但叶酸水平正常。所有 4 例患者均有颅底增厚的放射学证据,表明维生素 A 水平低。基因检测未发现任何相关的致病性变异。
维生素 A 缺乏是一种严重的营养缺乏形式,可导致严重的视力丧失,并有潜在的骨质增生和视神经受压,使营养性视神经病变恶化。通常还存在其他微量营养素缺乏,可能会有影响。自闭症患者的饮食受限,临床医生需要更加警惕维生素的补充。