先天性失明与自闭症谱系障碍（ASD）：诊断挑战与干预选择
Congenital blindness and autism spectrum disorder (ASD): diagnostic challenges and intervention options.
作者信息
Suhumaran Sharline, Yeleswarapu Sita Padmini, Daniel Lourdes Mary, Wong Chui Mae
机构信息
Department of Child Development, KK Women's and Children's Hospital, Singapore
Department of Child Development, KK Women's and Children's Hospital, Singapore.
出版信息
BMJ Case Rep. 2020 Feb 11;13(2):e232981. doi: 10.1136/bcr-2019-232981.
Abstract
The case of a 6-year-old boy with congenital blindness and features suggestive of autism spectrum disorder (ASD) is reported. He presented to a developmental paediatrician with global developmental delay, worsening self-injurious behaviours and difficulties in social interaction, transitions and interactive play. He demonstrated poor response to his name, rigidity, repetitive behaviours and had a sensory profile suggestive of ASD. This paper discusses the challenges in diagnosing and managing ASD in visually impaired children.
摘要
报告了一名6岁先天性失明男孩的病例，其具有自闭症谱系障碍（ASD）的特征。他因全面发育迟缓、自我伤害行为加重以及社交互动、转换和互动游戏方面的困难，就诊于一名发育儿科医生。他对自己名字反应不佳、行为刻板、有重复行为，且感觉特征提示患有ASD。本文讨论了在视力受损儿童中诊断和管理ASD的挑战。
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