Results 11 to 20 of about 524,713 (207)
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia [PDF]
Pediatric cataract is a leading cause of childhood blindness. This study aimed to determine the genetic cause of pediatric cataract in Australian families by screening known disease-associated genes using massively parallel sequencing technology.
Shari Javadiyan +14 more
doaj +6 more sources
Srijana Adhikari, Ujjowala D Shrestha Department of Pediatric Ophthalmology and Strabismus, Tilganga Institute of Ophthalmology, Kathmandu, Nepal Purpose: To assess the outcome of cataract surgery with hydrophilic acrylic intraocular lens (IOL ...
Adhikari S, Shrestha UD
doaj +1 more source
EPHA2 Polymorphisms and Age-Related Cataract in India [PDF]
Objective: We investigated whether previously reported single nucleotide polymorphisms (SNPs) of EPHA2 in European studies are associated with cataract in India. Methods: We carried out a population-based genetic association study. We enumerated randomly
Maraini, G +12 more
core +5 more sources
Secondary glaucoma after pediatric cataract surgery
AIM:To determine the incidence and risk factors of secondary glaucoma after pediatric cataract surgery. METHODS: Two hundred and forty nine eyes of 148 patients underwent cataract surgery without intraocular lens (IOL) implantation (group 1), and 220 ...
Yasin Çinar +7 more
doaj +2 more sources
Trypan blue-assisted posterior capsulorhexis in pediatric cataract surgery [PDF]
Ayman Lotfy,1,2 Ayman Abdelrahman1,2 1Ophthalmology Department, Zagazig University Hospital, 2Alpha Vision Center, Zagazig, Egypt Purpose: To evaluate the safety and efficacy of staining the posterior capsule with trypan blue during capsulorhexis in ...
Lotfy A, Abdelrahman A
doaj +1 more source
Purpose: To discuss the impact of COVID-19 pandemic on the pediatric cataract surgery services in a tertiary care institute in India, as well as the protocol followed for these surgeries.
Parul Chawla Gupta +6 more
doaj +1 more source
A deleterious variant of FCHSD1 results in mTOR pathway overactivation and may cause porto‐sinusoidal vascular disorder (PSVD). The pedigree of the family demonstrated an autosomal dominant disease with variable expressivity. Whole‐genome sequencing and Sanger sequencing both validated the existence of the FCHSD1 variant and the heterozygosity of c ...
Jingxuan Shan +19 more
wiley +1 more source
Purpose: The study sought to describe the clinical presentation pattern of pediatric cataracts and factors leading to delay in surgery at a tertiary care center in North India.
Sudarshan Khokhar +4 more
doaj +1 more source
Pre- and Post-Operative Intraocular Pressure of Pediatric Cataract Surgery
Introduction: Cataract is an eye lens opacification which prevents clear vision. It is the leading cause of blindness and vision impairment worldwide, including Indonesia.
Reyhana Khansa Mawardi +3 more
doaj +1 more source
Calcification of the intraocular lens is an uncommon phenomenon that usually follows an uncomplicated surgery. Here, the authors report the first case of a 66‐year‐old male patient who presented with defective vision and was diagnosed with sunflower ...
Kirandeep Kaur +2 more
doaj +1 more source

