Clinical and genetic spectrum of coloboma: A proposal for a comprehensive approach to pediatric patients [PDF]
Purpose to analyze pediatric coloboma cases to (1) identify ophthalmological and systemic associations, (2) establish the variables with the highest probability of reaching a genetic diagnosis and worse visual prognosis and (3) propose a clinical and ...
Baleta Riera, L. +11 more
core +1 more source
Background: Ocular B-mode ultrasonography (USG) acts as a valuable adjuvant for assessing the posterior segment of the eye in mature cataract, especially when fundus visualization is obscured by media opacities such as vitreous hemorrhage, asteroid ...
Athira Ajayghosh , Vageesha TM
doaj +1 more source
Proceedings 36th Symposium ESVN‐ECVN 12th‐14th September 2024
Journal of Veterinary Internal Medicine, Volume 38, Issue 6, Page 3461-3536, November/December 2024.
wiley +1 more source
Kosuke Abe,1,2 Jumi Shirane,2 Masuo Sakamoto,1 Fumi Tanabe,1 Kazuki Kuniyoshi,1 Chota Matsumoto,1 Yoshikazu Shimomura11Department of Ophthalmology, Kinki University Faculty of Medicine, Osaka-Sayama, Osaka, Japan; 2Nara Hospital, Kinki University Faculty
Abe K +6 more
doaj
Clinical Spectrum and Long-Term Anatomical and Functional Outcomes of Pars Plana Vitrectomy in Retinal Detachments Associated With Choroidal Coloboma. [PDF]
Kannan NB +4 more
europepmc +1 more source
Choroidal Coloboma Presenting as Leukocoria
Ilias Georgalas +3 more
openaire +3 more sources
Sequential Scanning Electron Microscopic Analyses of Normal and Spontaneously Occurring Abnormal Ocular Development in C57B1/6J Mice [PDF]
Embryos of C57B1/6J mice were examined grossly, and by light and scanning electron microscopy on days 8 through 19 of gestation. Adult eyes were examined by slit lamp biomicroscopy and light microscopy.
Cook, Cynthia S., Sulik, Kathleen K.
core +1 more source
Maculopatia Torpedo numa Criança Caucasiana de 5 Anos de Idade com Ambliopia Anisometrópica: Relato de Caso [PDF]
The aim of this study is to report a clinical case of asymptomatic female Caucasian children with torpedo maculopathy. A 5-year-old girl was referred to our clinic for routine evaluation.
Dutra-Medeiros, M +3 more
core
Pediatric Choroidal Coloboma with Macular Hole at the Edge of the Coloboma [PDF]
Pooja, Bansal +2 more
openaire +2 more sources
Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases. [PDF]
PurposeThis study was undertaken to identify causal mutations responsible for autosomal recessive retinitis pigmentosa (arRP) in consanguineous families.MethodsLarge consanguineous families were ascertained from the Punjab province of Pakistan.
Akram, Javed +11 more
core +1 more source

