Purpose: Stickler syndrome is an autosomal dominant inherited disorder that is well known to be highly associated with the development of rhegmatogenous retinal detachment.
Daisaku Kimura+9 more
doaj +1 more source
Purpose: to present our experience of surgical treatment of peripheral retinoschisis without macular involvement using a scleral buckle.Material and methods.
D. O. Shkvorchenko+4 more
doaj +1 more source
Vision-related Quality of Life and Visual Function after Retinal Detachment Surgery [PDF]
PurposeTo compare the vision-related quality of life (VR QOL) after rhegmatogenous retinal detachment (RD) surgery with that of normal controls and to investigate the relationship between the VR QOL and visual function after surgery for RD ...
Hiraoka Takahiro+7 more
core +1 more source
Assessment of chandelier-assisted scleral buckling surgery
Context Recently, there has been a shift towards the use of pars plana vitrectomy (PPV) as the first choice for rhegmatogenous retinal detachment (RRD) repair.
Mohsen A Abou Shousha
doaj +1 more source
Changes in Corneal Topography after 25-Gauge Transconjunctival Sutureless Vitrectomy versus after 20-Gauge Standard Vitrectomy [PDF]
journal ...
Hiraoka T.+7 more
core +1 more source
Retinopexia com "buckle" escleral e crioterapia guiada por ultrassom: relato de caso [PDF]
If the ocular media are clear, indirect binocular ophthalmoscopy allows retinal detachment and retinal tear identification and treatment under direct visualization.
FOLGOSA, Marco Sérgio Pinto Alves+4 more
core +2 more sources
Absorbable suture for band tightening of scleral buckling in pseudophakic rhegmatogenous retinal detachment: a modified surgical technique and a 6-month follow-up [PDF]
Background: Rhegmatogenous retinal detachment (RRD) is a separation of the neurosensory retina from the retinal pigment epithelium as a result of liquid vitreous passing through a retinal break.
Asadi-Moghaddam, Mahsa+3 more
core +3 more sources
Bilateral giant retinal tears in Osteogenesis Imperfecta. [PDF]
BACKGROUND: Osteogenesis imperfecta (OI) is a rare primarily autosomal dominant condition in which the connective tissues of bones, ligaments and sclerae do not form properly.
DeVile, Catherine+4 more
core +1 more source
Rare Infectious Diseases: Detection and Clinical Implications
Rare infectious diseases are infections that are uncommon, have a low incidence, and are caused by newly emerging pathogens, cross‐species or ectopic infections, or host immunodeficiencies. The detection and diagnosis of rare infections is one of the main reasons for misdiagnosis and missed diagnosis.
Xin Qian+7 more
wiley +1 more source
Chorioretinal Coloboma Complications: Retinal Detachment and Choroidal Neovascular Membrane [PDF]
PURPOSE: To report the chorioretinal coloboma, and its association with increased risk of retinal detachment (RD) and choroidal neovascularization (CNV).
Abbey, Ashkan M.+5 more
core +6 more sources