(1) Background: Albinism is characterized by a lack of pigment in eyes, hair, and skin and
developmental changes in the eye such as foveal hypoplasia. Patients require optical …

INTRODUCTION: Human albinism is a genetic condition associated with visual impairment
that affects many aspects of daily life. Office measurements of visual acuity do not …

Oculocutaneous albinism is an inherited disorder characterised by absent or minimal
production of a pigment called melanin. As a result, pigmentation is absent from or …

Introduction A number of vision defects have been reported in association with albinism,
such as photophobia, nystagmus and astigmatism. In many cases only prescription …

Purpose To describe the prevalence and severity of photosensitivity in patients with
albinism, and to compare with ocular features and how this correlated with use and choice of …

Individuals with ocular and oculocutaneous albinism (OCA) have significantly reduced
visual acuity (VA) resulting in visual impairment (VI). The aim is to report on the visual …

PURPOSE: All people with oculocutaneous albinism (OCA) have reduced vision. This study
aimed to assess the benefits of low vision aids for people with OCA. METHODS: Seventy …

We read with keen interest the recently published study titled “low-vision intervention for
oculocutaneous albinism in a tertiary eye care hospital in India” by Gopalakrishnan et al.[1] …

Albinism refers to a group of genetic disorders that, following genetic mutations, lead to
impaired melanin production, resulting in skin allergies and visual impairment in affected …

Purpose To evaluate the significance of sociodemographic and clinical variables on the
quality of life of low-vision patients in a tertiary hospital in Enugu, Nigeria, and also …