Results 71 to 80 of about 503,985 (221)

Intraocular Metastasis: Differential Diagnosis and Management

open access: yesClinical &Experimental Ophthalmology, Volume 54, Issue 3, Page 382-397, April 2026.
ABSTRACT Intraocular metastases represent the most common type of malignant intraocular tumour in adults. These commonly affect the choroid but can also involve the iris, ciliary body, retina, vitreous, optic disc or lens. Breast and lung cancer are the most common origins of intraocular metastases.
Genovefa Μachairoudia   +3 more
wiley   +1 more source

Glaucoma in a Suburban Tertiary Care Hospital in Nigeria

open access: yesJournal of Ophthalmic & Vision Research, 2010
Purpose: To determine the incidence and contribution of different types of glaucoma to blindness at Irrua Specialist Teaching Hospital, a suburban tertiary care hospital in Edo State, Nigeria.
Malachi Epo Enock   +2 more
doaj  

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 642-652, March 2026.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää   +14 more
wiley   +1 more source

Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma.

open access: yesOphthalmology (Rochester, Minn.), 2020
PURPOSE Developmental abnormalities of the ocular anterior segment in some cases can lead to ocular hypertension and glaucoma. CPAMD8 is a gene of unknown function recently associated with ocular anterior segment dysgenesis, myopia, and ectopia lentis ...
O. Siggs   +18 more
semanticscholar   +1 more source

Avances en la genética de los glaucomas Advances in glaucoma genetics

open access: yesRevista Cubana de Oftalmología, 1999
Con esta revisión los autores se han planteado el objetivo de motivar el interés de los oftalmólogos -en especial aquellos involucrados en el diagnóstico y tratamiento de los individuos afectados de glaucoma-, por conocer los avances genéticos de esta ...
Elier Ortiz González   +3 more
doaj  

Cataract surgery in juvenile xanthogranuloma: Case report and a brief review of literature

open access: yesIndian Journal of Ophthalmology, 2013
There is limited literature on the management of cataracts in juvenile xanthogranuloma (JXG). A 2-month-old girl presented to us with hyphema, secondary glaucoma OU and skin nodules suggestive of JXG.
R Muralidhar   +5 more
doaj   +1 more source

Optical coherence tomographic findings in optic nerve hypoplasia

open access: yesIndian Journal of Ophthalmology, 2013
We investigated a case of unilateral optic nerve hypoplasia using spectral domain optical coherence tomography (SDOCT). Optical coherence tomography was done on both eyes using 5-line Raster scan for the fovea to analyze the retinal nerve fiber layer ...
Daruchi Moon, Tae Kwann Park
doaj   +1 more source

A new Gujarati language logMAR visual acuity chart: Development and validation

open access: yesIndian Journal of Ophthalmology, 2013
Aims: Gujarati is the main spoken language of a large proportion of the population of India. The aim of this study was to develop and validate a new Minimum Angle of Resolution (logMAR) visual acuity chart in the Gujarati language. Materials and Methods:
Ananth Sailoganathan   +2 more
doaj   +1 more source

Is this really juvenile glaucoma?

open access: yesMalaysian Journal of Ophthalmology
Background: Pigmentary glaucoma (PG) is a clinical diagnosis characterised by liberation of pigments from the iris pigment epithelium into the anterior segment, with the evidence of glaucomatous optic neuropathy. Case presentation: A 34-year-old man presented with bilateral visual acuity of 6/9, normal anterior segment, intraocular pressure of 17 mmHg
Kah Suen Leng, Jie Jie Lim, Hong Kee Ng
openaire   +1 more source

Association of FOXC1 Duplications With Juvenile Open-Angle Glaucoma.

open access: yesJAMA ophthalmology
Importance While FOXC1 single-nucleotide variants and deletions are well-established causes of Axenfeld-Rieger syndrome, few FOXC1 duplications have been reported.
G. Maxwell   +17 more
semanticscholar   +1 more source

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