Results 51 to 60 of about 4,548 (218)
Ocular Hypotony Secondary to Spontaneously Ruptured Posterior Staphyloma [PDF]
Michael A, Mahr +3 more
openaire +3 more sources
Association between inferior posterior staphyloma on choroidal vessels running patterns in healthy eyes. [PDF]
Terasaki H +7 more
europepmc +3 more sources
Correlation between axial length and the elasticity of the posterior segment of eyeball in myopic eyes without posterior staphyloma: a shear wave elastography-based cross-sectional study. [PDF]
Qian T +6 more
europepmc +3 more sources
Giant anterior scleral staphyloma caused by blunt ocular trauma: a case report
Background Anterior scleral staphyloma is a relatively rare disease characterized by thinning and expansion of sclera. We described the clinical presentation, diagnosis and treatment of a case with giant anterior scleral staphyloma caused by blunt ocular
JinBo Chen +4 more
doaj +1 more source
Purpose: To compare morphological features of staphyloma (type and grade) with structural and functional outcomes in 11 patients with symptomatic myopic tractional maculopathy (MTM) who underwent macular buckle surgery.
Gitanjli Sood, Pradeep Susvar
doaj +1 more source
Background The objective is to examine the clinical characteristics of three patients with macular hole that occurred in inferior posterior staphyloma associated with tilted disc syndrome.
Hiroshi Mizuno +6 more
doaj +1 more source
Purpose: to describe a patient with a contractile peripapillary staphyloma and transient visual loss (TVL) that underwent repeated OCTA examination documenting disc contraction and increased peripapillary vessel density as the mechanism of TVL ...
Kenzo Hokazono +2 more
doaj +1 more source
Fundus changes in high myopic Kashmiri population
Background: High myopia (defined as myopia of -6D or more) is one of the main causes of visual impairment worldwide. High myopia is always accompanied by pathological structural changes such as axial elongation, posterior staphyloma, lacquer crack ...
Nazia Anjum +2 more
doaj +1 more source
Progression of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus [PDF]
BACKGROUND: Leber’s congenital amaurosis (LCA) accounts for 5% of inherited retinal disease and is usually inherited as an autosomal recessive trait. Genetic and clinical heterogeneity exist.
Inglehearn, C.F. +5 more
core +1 more source

