"My child can't see"-workup and management of children with low vision: a joint workshop of the AAPOS Low Vision Rehabilitation and Genetic Eye Diseases Committees
- PMID: 40441479
- PMCID: PMC12185237
- DOI: 10.1016/j.jaapos.2025.104229
"My child can't see"-workup and management of children with low vision: a joint workshop of the AAPOS Low Vision Rehabilitation and Genetic Eye Diseases Committees
Abstract
Children with visual impairment present a unique challenge to pediatric ophthalmologists. Diagnostic workup may include tests that require specialized interpretation, such as genetic testing and neuropsychological assessments. The differential diagnosis includes rare conditions, such as certain inherited retinal disorders, as well as more common conditions, such as cerebral/cortical visual impairment. Management of children with visual impairment requires ophthalmologists to become familiar with visual prognosis associated with various conditions and supports available for children with low vision, which vary by age. Younger children benefit from early intervention services, which may include pre-braille skills and orientation and mobility training. Older children require counseling with regard to driving, independent skills, and transition to adult care. This workshop provides detailed discussion of differential diagnoses, diagnostic tests, and management strategies in infants and older children with visual impairment. We emphasize the importance of a multidisciplinary approach, since vision impacts development in multiple domains, and many children with visual impairments are multiply disabled.
Copyright © 2025 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.
Similar articles
-
Reading aids for adults with low vision.Cochrane Database Syst Rev. 2018 Apr 17;4(4):CD003303. doi: 10.1002/14651858.CD003303.pub4. Cochrane Database Syst Rev. 2018. PMID: 29664159 Free PMC article.
-
Surgical interventions for bilateral congenital cataract in children aged two years and under.Cochrane Database Syst Rev. 2022 Sep 15;9(9):CD003171. doi: 10.1002/14651858.CD003171.pub3. Cochrane Database Syst Rev. 2022. PMID: 36107778 Free PMC article.
-
Signs and symptoms to determine if a patient presenting in primary care or hospital outpatient settings has COVID-19.Cochrane Database Syst Rev. 2022 May 20;5(5):CD013665. doi: 10.1002/14651858.CD013665.pub3. Cochrane Database Syst Rev. 2022. PMID: 35593186 Free PMC article.
-
Community screening for visual impairment in older people.Cochrane Database Syst Rev. 2018 Feb 20;2(2):CD001054. doi: 10.1002/14651858.CD001054.pub3. Cochrane Database Syst Rev. 2018. PMID: 29460275 Free PMC article.
-
Orientation and mobility training for adults with low vision.Cochrane Database Syst Rev. 2010 May 12;2010(5):CD003925. doi: 10.1002/14651858.CD003925.pub3. Cochrane Database Syst Rev. 2010. PMID: 20464725 Free PMC article.
References
-
- Lorenz B, Gyurus P, Preising M, et al. Early-onset severe rod-cone dystrophy in young children with RPE65 mutations. Invest Ophthalmol Vis Sci 2000;41:2735–42. - PubMed
-
- Felius J, Thompson DA, Khan NW, et al. Clinical course and visual function in a family with mutations in the RPE65 gene. Arch Ophthalmol 2002;120:55–61. - PubMed
-
- Tsang SH, Sharma T. Leber congenital amaurosis. Adv Exp Med Biol 2018;1085:131–7. - PubMed
-
- Whiting S, Jan JE, Wong PK, Flodmark O, Farrell K, McCormick AQ. Permanent cortical visual impairment in children. Dev Med Child Neurol 1985;27:730–39. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources