PurposeTo investigate the time-course of foveal development after birth in infants with albinism.DesignProspective, comparative cohort optical coherence tomography (OCT) studyMethods36 children with albinism were recruited. All participants were aged between 0 and 6 years and were seen at Leicester Royal Infirmary. A total of 181 mixed cross-sectional and longitudinal OCT examinations were obtained, which were analyzed for differences in retinal development in comparison to 297 cross-sectional control examinations.ResultsNormal retinal development involves migration of the inner retinal layers (IRLs) away from the fovea, migration of the cone photoreceptors into the fovea and elongation of the outer retinal layers (ORLs) over time. In contr...
Purpose: The purpose of this study was to examine the onset and progression of with-the-rule (WTR) a...
Purpose : Evidence of ongoing retinal development in children with albinism has been demonstrated. L...
Purpose: Albinism is a rare genetic disorder of melanin production, which can affect only eyes or si...
The three aims of this study were to:• Investigate the postnatal development of the optic nerve head...
Albinism is an uncommon genetic condition characterised by hypopigmentation of the hair, skin and ey...
AbstractAlbinism, an inherited disorder of melanin biosynthesis, disrupts normal retinal development...
Albinism refers to a group of genetic abnormalities that are associated with profound defects throug...
Purpose: To characterize the time course of normal foveal development in vivo in term infants and yo...
Normally, postnatal development of the human retina involves centrifugal displacement of the inner r...
Purpose: The main aims were to: 1) characterise the morphology of the iris structures and investigat...
Introduction: Individuals with albinism and IIN demonstrate retinal structural abnormalities. Howeve...
We present handheld optical coherence tomography (OCT) diagnosis of Grade 4 foveal hypoplasia (fovea...
Background/aims: To compare interocular acuity differences, crowding ratios, and binocular summation...
Background: Optical coherence tomography (OCT), multifocal electroretinography (mfERG) and full-fiel...
Background: The purpose of the study was to compare morphological retinal differences in children wi...
Purpose: The purpose of this study was to examine the onset and progression of with-the-rule (WTR) a...
Purpose : Evidence of ongoing retinal development in children with albinism has been demonstrated. L...
Purpose: Albinism is a rare genetic disorder of melanin production, which can affect only eyes or si...
The three aims of this study were to:• Investigate the postnatal development of the optic nerve head...
Albinism is an uncommon genetic condition characterised by hypopigmentation of the hair, skin and ey...
AbstractAlbinism, an inherited disorder of melanin biosynthesis, disrupts normal retinal development...
Albinism refers to a group of genetic abnormalities that are associated with profound defects throug...
Purpose: To characterize the time course of normal foveal development in vivo in term infants and yo...
Normally, postnatal development of the human retina involves centrifugal displacement of the inner r...
Purpose: The main aims were to: 1) characterise the morphology of the iris structures and investigat...
Introduction: Individuals with albinism and IIN demonstrate retinal structural abnormalities. Howeve...
We present handheld optical coherence tomography (OCT) diagnosis of Grade 4 foveal hypoplasia (fovea...
Background/aims: To compare interocular acuity differences, crowding ratios, and binocular summation...
Background: Optical coherence tomography (OCT), multifocal electroretinography (mfERG) and full-fiel...
Background: The purpose of the study was to compare morphological retinal differences in children wi...
Purpose: The purpose of this study was to examine the onset and progression of with-the-rule (WTR) a...
Purpose : Evidence of ongoing retinal development in children with albinism has been demonstrated. L...
Purpose: Albinism is a rare genetic disorder of melanin production, which can affect only eyes or si...