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Pagina 1 a partire dal 21 risultati
Unilateral acute hydrops in a child with bilateral microcornea and iridofundal coloboma.
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A 15-year-old female child with history of bilateral poor vision since childhood presented with sudden onset pain, photophobia, and diminution of vision OD for 10 days. Visual acuity was hand motion OD and 1/60 OS. Slit lamp examination revealed microcornea OU with multiple intrastromal fluid clefts
Unilateral cataract with lens coloboma and bilateral corneal edema in a guanaco.
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Dexamethasone Implant Migration through an Iris Coloboma.
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Ozurdex® 0.7 mg (dexamethasone 0.7 mg implant, Allergan, Dublin, Ireland), an intravitreal biodegradable implant, is indicated for cystoid macular edema due to various causes. One of its known and uncommon complications is implant migration to the anterior chamber, causing corneal edema that, in
Hypotonic maculopathy secondary to scleral defect in atypical retinochoroidal coloboma.
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OBJECTIVE
To describe a patient with unilateral hypotonic maculopathy and optic disc edema after spontaneous bulbar perforation of a full-thickness scleral defect.
METHODS
An 11-year-old girl underwent scleral buckling surgery. Preoperative and postoperative evaluation included optical coherence
Cataract surgery outcomes in eyes with chorioretinal coloboma.
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[Anesthesia in a patient with Treacher-Collins syndrome].
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Treacher Collins syndrome is a form of mandibulofacial dysostosis characterized by deafness, hypoplasia of facial bones (mandible, maxilla and cheek bone), antimongoloid slant of palpebral fissures, coloboma of the lower lid and bilateral anomalies of auricle. The condition may be associated with
[Maculopathy with optic nerve pits : Morphological criteria in SD-OCT].
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Optic pit is a congenital anomaly with malformation similar to coloboma of the optic disc. The cause of optic pit maculopathy is controversial. We used high resolution OCT to investigate changes in the vitreoretinal and vitreopapillary transition within optic pit eyes.
The vitreoretinal and
Scanning electron microscope evaluation of the corneal endothelium in a case of unilateral microphthalmos with retrobulbar cyst in the pigmented rabbit.
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A case of unilateral microphthalmos with a sizeable retrobulbar cyst, totally dysplastic retina, and gross nerve head coloboma is reported in an otherwise normal pigmented rabbit. Despite the gross abnormality of the posterior part of the globe, an iris sectoral coloboma, and abnormal lentoid body,
Scleral Cyst Associated with Anomalous Tilted Configuration of the Optic Nerve Head: A Case Report.
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There is limited published data currently available on scleral cysts in the posterior pole. Here, we detail the case of a patient who was suspected to have a peripapillary scleral cyst imprinting the optic nerve head (ONH) profile. The 52-year-old asymptomatic and otherwise healthy woman presented
Clinical Presentation and Management Outcomes of Coexistent Congenital Glaucoma and Retinopathy of Prematurity.
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OBJECTIVE
The purpose of this study was to report presentation and outcomes of coexisting congenital glaucoma with retinopathy of prematurity (ROP) in "Indian Twin cities ROP study (ITCROPS)."
METHODS
Children with ROP and congenital glaucoma were identified from ITCROPS (prospective digital
Outcomes of primary combined trabeculotomy and trabeculectomy in early onset glaucoma in children with congenital aniridia
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Purpose: To report clinical features and treatment outcomes of primary combined trabeculotomy with trabeculectomy (CTT) in congenital aniridia with glaucoma in children aged 3 years or less.
Design:
Quantitative brain morphological analysis in CHARGE syndrome.
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CHARGE syndrome (CS) is a rare congenital syndrome characterized by coloboma, heart anomaly, choanal atresia, retardation of growth and development, and genital and ear anomalies. While several neuroimaging studies have revealed abnormalities such as hypoplasia of the semicircular canal, olfactory
[Perception of the blind spot with Rauschfeld campimetry. An additional diagnostic criterion in papillary changes].
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In conventional test point perimetry the optic disc is detected as an absolute scotoma (blind spot). However, in white noise campimetry the blind spot usually cannot be perceived: the white noise is continuous over the whole field if presented to a normal eye. This is true not only for the blind
Prosthetic iris implantation for congenital, traumatic, or functional iris deficiencies.
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OBJECTIVE
To determine the efficacy and safety of surgical implantation of prosthetic iris devices in patients with anatomic or functional iris deficiencies.
METHODS
Cincinnati Eye Institute, Cincinnati, Ohio, USA.
METHODS
Twenty-five patients were enrolled in an interventional prospective
[Special indications for endocapsular artificial lens implantation].
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Report on the successful endocapsular fixation of a posterior chamber lens in two young patients with ocular anomalies (lamellar cataract and large total iridectomy; nuclear cataract and normotensive congenital glaucoma), in whom lens with chamber angle or sulcus fixation lens would have been
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