scholarly journals Motion Processing Deficits in Children With Cerebral Visual Impairment and Good Visual Acuity

2021 ◽  
Vol 62 (14) ◽  
pp. 12
Author(s):  
Arvind Chandna ◽  
Nikolay Nichiporuk ◽  
Spero Nicholas ◽  
Ram Kumar ◽  
Anthony M. Norcia
Strabismus ◽  
2012 ◽  
Vol 20 (2) ◽  
pp. 78-83 ◽  
Author(s):  
Maria van Genderen ◽  
Marjoke Dekker ◽  
Florine Pilon ◽  
Irmgard Bals

2021 ◽  
Vol 15 ◽  
Author(s):  
Arvind Chandna ◽  
Saeideh Ghahghaei ◽  
Susan Foster ◽  
Ram Kumar

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.


2017 ◽  
Vol 10 (2) ◽  
pp. 95-103
Author(s):  
Ymie J. van der Zee ◽  
Peter Stiers ◽  
Heleen M. Evenhuis

2011 ◽  
Vol 54 (7) ◽  
pp. e1-e8 ◽  
Author(s):  
JOEL M WEINSTEIN ◽  
RICK O GILMORE ◽  
SUMERA M SHAIKH ◽  
ALLEN R KUNSELMAN ◽  
WILLIAM V TRESCHER ◽  
...  

Author(s):  
Joel M. Weinstein ◽  
Rick O. Gilmore ◽  
Sumera Shaikh ◽  
Jeremy Fesi ◽  
Tashima Lauren ◽  
...  

2012 ◽  
Vol 54 (7) ◽  
pp. 662-662 ◽  
Author(s):  
JOEL M WEINSTEIN ◽  
RICK O GILMORE ◽  
SUMERA M SHAIKH ◽  
ALLEN R KUNSELMAN ◽  
WILLIAM V TRESCHER ◽  
...  

2021 ◽  
Vol 15 ◽  
Author(s):  
Sruti Raja ◽  
Batool Sahar Emadi ◽  
Eric D. Gaier ◽  
Ryan A. Gise ◽  
Anne B. Fulton ◽  
...  

Cerebral visual impairment (CVI) is a leading cause of visual impairment in children in developed countries, but diagnostic tools to detect CVI are limited. We sought to analyze the visual acuity of children with CVI as assessed by visual evoked potentials (VEPs) and preferential looking test (PLT) to determine whether the relationship between the visual outcomes on these two testing methods may serve as a biomarker of CVI. We performed a retrospective chart review of patients with a confirmed diagnosis of CVI and at least one ophthalmological assessment with visual acuity measured by VEP and PLT. Of the 218 patients included in the study, the most common condition associated with CVI was an underlying genetic disorder (36%, 79/218). Treatment for seizures occurred in the majority of the entire cohort of patients (80%, 175/218). Ophthalmic comorbidities included retinal disease in 23 patients, optic nerve disease in 68 patients, nystagmus in 78 patients, and strabismus in 176 patients. When assessed by either VEP or PLT, visual acuity in children with CVI fell below expected norms. At initial and final presentations, VEP acuity exceeded PLT acuity by one or more octaves, and this difference was greater than expected compared with normal visual development. We propose utilizing this quantifiable disparity between VEP and PLT as a biomarker of CVI.


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