Results 91 to 100 of about 7,339 (214)

The juvenile glaucoma gene on 1q21-q31 is not associated with primary open angle glaucoma (POAG)

open access: yes, 1996
Purpose: One locus for a form of juvenile primary open angle glaucoma has been mapped to the 1q21-q31 region of human chromosome 1. To determine if adult onset primary open angle glaucoma (POAG) is also caused by mutations a gene located in this region ...
Youn, J.   +9 more
core  

Glaucoma (Nursing)

open access: yes, 2022
Glaucoma is the second leading cause of permanent blindness in the United States and occurs most often in older adults. There are four general categories of adult glaucoma: primary open-angle and angle-closure, and the secondary open and ...
Havens, Shane J   +3 more
core   +1 more source

Comparison of visual field test results obtained through Humphrey matrix frequency doubling technology perimetry versus standard automated perimetry in healthy children

open access: yesIndian Journal of Ophthalmology, 2013
Aims : The aim of this study was to compare the visual field test results in healthy children obtained via the Humphrey matrix 24-2 threshold program and standard automated perimetry (SAP) using the Swedish interactive threshold algorithm (SITA)-Standard
Sibel Kocabeyoglu   +5 more
doaj   +1 more source

Clinical Features of Juvenile Open-angle Glaucoma

open access: yesOftalʹmologiâ
Juvenile open-angle glaucoma (JOAG) is a genetically determined disease of young age, which is diagnosed before the 40, which is based on anomalies in the structure of the drainage system of the eye.Objective: to identify the features of morphometric and
A. V. Malyshev   +6 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

Management of primary childhood glaucoma: Evaluation of practice, practice gaps, and needs in a low-resource country

open access: yesThe Pan-American Journal of Ophthalmology
Purpose: To evaluate the current practice, equipment availability, and training needs for managing childhood glaucoma in Nigeria. Materials and Methods: An online questionnaire (Google Forms) was distributed through E-mails and social media platforms of ...
Mary Ugalahi   +6 more
doaj   +1 more source

[Diagnostic image (106). A girl with blurred vision. Unilateral juvenile glaucoma with ectropion uveae]

open access: yes, 2002
Contains fulltext : 165267.pdf (Publisher’s version ) (Open Access)A 10-year-old girl showed ectropion uveae of the iris of her right eye.
Cruysberg, J.R.M., Nobacht, S.
core  

Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31

open access: yes, 1996
A locus for autosomal dominant juvenile onset primary open angle glaucoma (POAG) was recently assigned to chromosome region 1q21-q31. In the present study, a large Greek family with autosomal dominant adult onset POAG was investigated using ...
Psilas, K   +7 more
core   +1 more source

Cleft catastrophe following minimally invasive glaucoma surgery: Case report and review of literature

open access: yesIndian Journal of Ophthalmology. Case Reports
We present two cases of cyclodialysis cleft (CDC) following minimally invasive glaucoma surgery, both unresponsive to conservative treatment. The first, a 50-year-old man with prior vitreoretinal surgery, developed CDC post gonioscopy-assisted ...
Anand K Pathak   +4 more
doaj   +1 more source

Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene

open access: yes, 2002
“Early-onset glaucoma” refers to genetically heterogeneous conditions for which glaucoma manifests at age 5–40 years and for which only a small subset is molecularly characterized.
Buys, Yvonne   +15 more
core   +1 more source

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