Results 81 to 90 of about 36,217 (207)
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutations. It classically manifests with renal hypodysplasia and optic nerve anomalies. However, recent literature suggests an expanding phenotypic spectrum.
Nadira Sultana +2 more
wiley +1 more source
An action video game for the treatment of amblyopia in children: A feasibility study
Vision Research, 2018 HighlightsPlaying a custom child friendly action videogame resulted in improved visual acuity.Improvement of 1.4 lines after 20 h compared to more than 100 h of patching.The action videogame approach may be an effective adjunct treatment for amblyopia ...
Christina Gambacorta +6 more
semanticscholar +1 more source
CNS Neuroscience &Therapeutics, Volume 32, Issue 2, February 2026.The diagnostic model combining orbital and intracranial MAP‐MRI parameters could significantly optimize diagnostic efficiency of dysthyroid optic neuropathy. Comprehensive MAP‐MRI parameters analysis of the entire visual pathway enables a deeper understanding of disease involvement, provides novel insights into the early accurate diagnosis and ...
Mengsha Zou +7 more
wiley +1 more source
Community outreach: An indicator for assessment of prevalence of amblyopia
Indian Journal of Ophthalmology, 2018 Purpose: To study the prevalence, determine the magnitude, and cause of amblyopia among the children aged 6 months to 16 years in Kamrup district, Assam, India.
Damaris Magdalene +6 more
doaj +1 more source
The functional impact of amblyopia
Clinical and experimental optometry, 2018 Amblyopia is the most common disorder managed in paediatric ophthalmic practice in industrialised countries. Reports on the impact of amblyopia on tasks relevant to the activities of children, or on skills pertinent to their education and quality of life,
A. Webber
semanticscholar +1 more source
Genetic Pigmentary Disorders: From Molecular Mechanisms to Clinical Manifestations
The Journal of Dermatology, Volume 53, Issue 2, Page 169-179, February 2026.ABSTRACT Genetic pigmentary disorders represent a diverse group of genetic conditions characterized by alterations in melanin production and transport and melanocyte development, resulting from single‐gene pathological variants. These disorders encompass both hypopigmentary and hyperpigmentary phenotypes, affecting not only skin pigmentation but also ...
Ken Okamura, Tamio Suzuki
wiley +1 more source
Journal of Multidisciplinary HealthcareMo Y, Zhang H, Yu X, et al. J Multidiscip Healthc. 2025;18:459–468. Page 461, Ethical Consideration and Data Collection Procedure section, line 2, the text “(No. 2023KYPJ271)” should read “(No.
Mo Y +6 more
doaj
Amblyopia screening in children in Bandar Abbas (Iran) during 2011–2012
Electronic Physician, 2014 Background: Amblyopia is an acquired defect of vision caused by abnormal visual experience that occurs during childhood. Since early diagnosis is important in preventing further irreparable effects, the aim of this study was to investigate the outcome ...
Ali Safari Moradabadi +6 more
doaj +1 more source
‘It’s too late’. Is it really? Considerations for amblyopia treatment in older children
Therapeutic Advances in Ophthalmology, 2019 In recent years, media coverage has demonstrated instances in which families of children aged 7 and older, newly diagnosed with strabismic and/or anisometropic amblyopia through community eyecare services, were told it was ‘too late’ for their child to ...
Marianne E.F. Piano, Anita J. Simmers
doaj +1 more source
Vojnosanitetski pregled, 2007 <zakljucak> S obzirom na neujednacenu pokrivenost zemlje oftamoloskom sluzbom, resurse i edukaciju trebalo bi usmeriti, pre svega, na pedijatre i lekare opste medicine koji su ukljuceni u pregled ociju dece. Takodje, bila bi potrebna standardizacija optotipa i protokola ispitivanja.
openaire +3 more sources