Results 11 to 20 of about 69 (59)
Refractive Accuracy of a Novel Swept‐Source OCT in Patients With Short and Long Eyes
Purpose: To analyze the refractive accuracy of a novel swept‐source optical coherence biometer (SS‐OCT), that uses individual refractive indices to measure axial length, in short and long eyes implanted with monofocal intraocular lenses (IOLs). Methods: This retrospective comparative study considered eyes with short axial length (AL) (< 22.5 mm) or ...
Laureano A. Rementería-Capelo+4 more
wiley +1 more source
Novel causative variants in Legius syndrome: SPRED1 Genotype spectrum expansion
Abstract Legius syndrome, commonly referred to as SPRED1‐related neurofibromatosis type 1‐like syndrome, is a rare autosomal dominant disorder characterized by café‐au‐lait macules, freckling, lipomas, macrocephaly, and heterogeneous neurodevelopmental manifestations, including a different degree of learning difficulties.
Cristina Chelleri+11 more
wiley +1 more source
2024 UK and Ireland modified Delphi consensus on myopia management in children and young people
Abstract Introduction This work aimed to establish the largest UK and Ireland consensus on myopia management in children and young people (CYP). Methods A modified Delphi consensus was conducted with a panel of 34 optometrists and ophthalmologists with expertise in myopia management.
Annegret H. Dahlmann‐Noor+34 more
wiley +1 more source
Abstract The objective was to evaluate the progression and management of eyelid tacking sutures before permanent eyelid surgical correction. A 1‐year‐old Aberdeen black Angus bull presented with a 1‐month history of bilateral corneal ulcers. Ophthalmic examination revealed an infected stromal corneal ulcer on the left eye and bilateral lower eyelid ...
Leila Bedos+4 more
wiley +1 more source
Phenotypic characteristics of Danish patients with achromatopsia
Abstract Purpose To describe the phenotype of Danish patients with genetically verified achromatopsia (ACHM) with special focus on signs of progression on structural or functional parameters, and possible genotype–phenotype correlations. Methods Forty‐eight patients were identified, with disease‐causing variants in five different genes: CNGA3, CNGB3 ...
Mette K. G. Andersen+4 more
wiley +1 more source
Intraocular Parafilaria bovicola infection and surgical removal in a mixed breed heifer
Abstract An approximately 1.5‐year‐old mixed breed heifer was presented for evaluation and treatment due to ocular pain affecting the right eye secondary to a live nematode within the anterior chamber. Ophthalmic examination revealed marked blepharospasm, evidence of chronic keratitis, uveitis, and a single, white, approximately 2.5 cm long, 0.5 mm ...
A. K. Shukla+5 more
wiley +1 more source
Abstract Background Toxoplasmosis is a parasitic infection caused by Toxoplasma gondii and is responsible for gestational and congenital infections worldwide. The current standard therapy is based on the administration of Spiramycin to prevent trans‐placental transmission. Other therapies are being studied to reduce the rates of foetal transmission and
Marco De Santis+8 more
wiley +1 more source
Extended phenotypic characterization of a novel Helsmoortel‐van der Aa syndrome case series
Abstract The neurodevelopmental disorder known as Helsmoortel‐van der Aa syndrome (HVDAS, MIM#616580) or ADNP syndrome (Orphanet, ORPHA:404448) is a multiple congenital anomaly (MCA) condition, reported as a syndrome in 2014, associated with deleterious variants in the ADNP gene (activity‐dependent neuroprotective protein; MIM*611386) in several ...
Giulia Pascolini+4 more
wiley +1 more source
Polarized light and the human fundus oculi
1. Measurements were made of the relative fractions of diffuse and specular reflexions in the fovea and periphery of the human fundus oculi.2. All the light emerging from the eye is scattered or reflected behind the receptors as bleaching the retina affects both fractions equally.3.
openaire +3 more sources
Mechanisms of cone sensitivity loss in retinitis pigmentosa
Abstract Purpose To explore the mechanisms of cone sensitivity loss in retinitis pigmentosa by combining two‐colour perimetry with threshold versus intensity (tvi) testing. Methods Seven subjects with autosomal recessive retinitis pigmentosa and 10 normal subjects were recruited and underwent perimetric testing of one eye using 480‐ and 640‐nm Goldman ...
Matthew P. Simunovic, Zaid Mammo
wiley +1 more source