PURPOSE: Treatment of the capillary vascular malformation (port-wine stain) in Sturge-Weber
syndrome with the use of a laser is helpful cosmetically. However, concerns have been …

Purpose To report the relative frequencies of childhood and early onset glaucoma subtypes
and their genetic findings in a large single cohort. Design Retrospective clinical and …

Purpose Developmental abnormalities of the ocular anterior segment in some cases can
lead to ocular hypertension and glaucoma. CPAMD8 is a gene of unknown function recently …

Study Objectives This study investigated the differences in melatonin circadian timing and
output, sleep characteristics, and cognitive function in myopic and non-myopic (or emmetropic…

Purpose ADAMTSL4-associated ectopia lentis is a rare autosomal recessive condition that
is primarily associated with crystalline lens displacement. However, the prevalence of other …

We report a case of microphthalmia, inferior adherent leukoma, and optic nerve hypoplasia
in an infant whose mother underwent biliopancreatic diversion surgery for obesity 7 years …

Congenital cataract is a rare but severe paediatric visual impediment, often caused by variants
in one of several crystallin genes that produce the bulk of structural proteins in the lens. …

Axenfeld-Rieger syndrome is an autosomal dominant condition associated with multisystemic
features including developmental anomalies of the anterior segment of the eye. Single …

Idiopathic intracranial hypertension can cause severe optic nerve damage with irreversible
visual loss. Heidelberg retina tomography is a sensitive and reproducible tool that can be …

Background Criteria for screening preterm infants for retinopathy of prematurity vary around
the world. We aimed to analyse the efficacy of alternative screening criteria. Design We …