Congenital blindness and autism spectrum disorder (ASD): diagnostic challenges and intervention options

被引：2

作者：

Suhumaran, Sharline ^{[1
]}

Yeleswarapu, Sita Padmini ^{[1
]}

Daniel, Lourdes Mary ^{[1
]}

Wong, Chui Mae ^{[1
]}

机构：

[1] KK Womens & Childrens Hosp, Dept Child Dev, Singapore, Singapore

来源：

BMJ CASE REPORTS | 2020年 / 13卷 / 02期

关键词：

child and adolescent psychiatry (paediatrics); developmental paediatrocs; NERVE HYPOPLASIA; CHILDREN; PREVALENCE;

D O I：

10.1136/bcr-2019-232981

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页数：5

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