Results 41 to 50 of about 62,480 (319)
Ocular manifestations in Gorlin-Goltz syndrome [PDF]
Background: Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare genetic disorder that is transmitted in an autosomal dominant manner with complete penetrance and variable expressivity.
Franzone, F.+8 more
core +1 more source
Spectrum of eye disorders seen in a pediatric eye clinic South East Nigeria
Purpose: This study aims to determine the prevalence, pattern, and time of presentation for the ocular disorders seen among children attending a pediatric eye clinic in Nigeria.
Eberechukwu O Achigbu+2 more
doaj +1 more source
Aim: The aim of this study was to evaluate the correlation between malocclusions and visual defects. This is a case-control study evaluating the prevalence of visual defects in patients with different types of malocclusions.
Cristina Grippaudo+4 more
doaj +1 more source
Clues from Crouzon: Insights into the potential role of growth factors in the pathogenesis of myelinated retinal nerve fibers. [PDF]
PurposeWe present a case of bilateral extensive peripapillary myelinated retinal nerve fibers (MRNF) in an individual with Crouzon syndrome, an inherited form of craniosynostosis caused by overactivation of fibroblast growth factor receptor 2.
Akil, Handan+5 more
core +3 more sources
Eye Segmentation Method for Telehealth: Application to the Myasthenia Gravis Physical Examination
Due to the precautions put in place during the COVID-19 pandemic, utilization of telemedicine has increased quickly for patient care and clinical trials.
Quentin Lesport+6 more
doaj +1 more source
Vision problems following stroke: developing a best practice statement [PDF]
An estimated 15 million people worldwide suffer a stroke each year, and in developed countries, survival is increasing. Of those who survive 30 days or more after their first event, many experience stroke-related vision and visual problems.
Stanley, Jennifer, Tolmie, Elizabeth
core +1 more source
Mitochondrial neurogastrointestinal encephalomyopathy: approaches to diagnosis and treatment [PDF]
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an ultra-rare disease caused by mutations in TYMP, the gene encoding for the enzyme thymidine phosphorylase.
Bax, BE
core +1 more source
Diplopia and eye movement disorders.
Published ...
Danchaivijitr, C, Kennard, C
core +2 more sources
Introduction: Congenital muscular torticollis (CMT) is the most common cause of torticollis in infants; other causes, including osseous, ocular, and central nervous system torticollis can easily be overlooked.
Min-Wook Kim+5 more
doaj +1 more source
Post-stroke visual impairment: a systematic literature review of types and recovery of visual conditions [PDF]
Aim: The aim of this literature review was to determine the reported incidence and prevalence of visual impairment due to stroke for all visual conditions including central vision loss, visual field loss, eye movement problems and visual perception ...
Currie, Jim+6 more
core +2 more sources