Higher Visual Function Deficits in Children With Cerebral Visual Impairment and Good Visual Acuity

In clinical practice Cerebral Visual Impairment (CVI) is typically diagnosed by observation of abnormal visually guided behaviors which indicate higher visual function deficits (HVFDs) suggesting abnormal brain development or brain damage in a child with a suitable clinical history. HVFDs can occur...

Full description

Bibliographic Details
Main Authors: Chandna, A. (Author), Foster, S. (Author), Ghahghaei, S. (Author), Kumar, R. (Author)
Format: Article
Language:English
Published: Frontiers Media S.A. 2021
Subjects:
Online Access:View Fulltext in Publisher
LEADER 03314nam a2200505Ia 4500
001 10.3389-fnhum.2021.711873
008 220427s2021 CNT 000 0 und d
020 |a 16625161 (ISSN) 
245 1 0 |a Higher Visual Function Deficits in Children With Cerebral Visual Impairment and Good Visual Acuity 
260 0 |b Frontiers Media S.A.  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.3389/fnhum.2021.711873 
520 3 |a In clinical practice Cerebral Visual Impairment (CVI) is typically diagnosed by observation of abnormal visually guided behaviors which indicate higher visual function deficits (HVFDs) suggesting abnormal brain development or brain damage in a child with a suitable clinical history. HVFDs can occur even in the presence of good visual acuity and may remain undiagnosed because the good visual acuity does not prompt further investigation. This leads to a lack of understanding of the child’s visual perceptual difficulties. In a prospective study, we determined the spectrum of HVFDs in a group of children with history suggestive of brain damage or disruption of brain development and an independent diagnosis of CVI in comparison with typically developing children with a structured 51 question inventory, the Higher Visual Function Question Inventory (HVFQI-51) adapted from the Cerebral Vision Impairment Inventory, CVI-I. Here, we show that the HVFQI-51 can detect a range of HVFDs in children with CVI with good visual acuity and clearly distinguishes these children from typically developing children. HVFDs in our study group could mostly be attributed to dorsal stream visual processing dysfunction though the spectrum varied between children. We report on the inclusion of the “not applicable” response option in analysis providing a picture of HVFDs more in tune with the overall disability of each child. We also propose a subset of 11 questions (Top-11) which discriminate between children with CVI vs. behaviors seen in typical children: this provides both a potential screening tool for initial assessment of HVFDs and a measure of CVI-related impairment, and needs further validation in a secondary independent sample. Copyright © 2021 Chandna, Ghahghaei, Foster and Kumar. 
650 0 4 |a adolescent 
650 0 4 |a Article 
650 0 4 |a brain damage 
650 0 4 |a brain development 
650 0 4 |a cerebral visual impairment 
650 0 4 |a cerebral visual impairment (CVI) 
650 0 4 |a child 
650 0 4 |a child behavior 
650 0 4 |a child development 
650 0 4 |a children 
650 0 4 |a clinical article 
650 0 4 |a controlled study 
650 0 4 |a disability 
650 0 4 |a eye disease assessment 
650 0 4 |a female 
650 0 4 |a good visual acuity 
650 0 4 |a higher visual function deficits 
650 0 4 |a Higher Visual Function Question Inventory 51 
650 0 4 |a human 
650 0 4 |a low vision 
650 0 4 |a male 
650 0 4 |a mass screening 
650 0 4 |a prospective study 
650 0 4 |a questionnaire 
650 0 4 |a screening 
650 0 4 |a structured question inventory 
650 0 4 |a visual acuity 
650 0 4 |a visual disorder 
700 1 |a Chandna, A.  |e author 
700 1 |a Foster, S.  |e author 
700 1 |a Ghahghaei, S.  |e author 
700 1 |a Kumar, R.  |e author 
773 |t Frontiers in Human Neuroscience