Results 11 to 20 of about 13,246 (176)

Childhood glaucoma profile in a Southwestern Ethiopia tertiary care center: a retrospective study [PDF]

open access: yesBMC Ophthalmology
Background Childhood glaucoma is a major cause of childhood blindness worldwide. The profile of childhood glaucoma has not been well characterized in sub-Saharan Africa.
Tarekegn Mulugeta   +2 more
doaj   +2 more sources

Profile of primary childhood glaucoma at a child eye health tertiary facility in Malawi [PDF]

open access: yesBMC Ophthalmology, 2022
Background To describe the clinical characteristics and treatment of primary childhood glaucoma at Queen Elizabeth Central Hospital in Blantyre, Malawi. Methods A retrospective case notes review was undertaken of all medical records of patients aged less
Shaffi Mdala   +7 more
doaj   +2 more sources

Changes of Peripapillary Retinal Nerve Fiber Layer in Childhood Glaucoma: A Systematic Review and Meta-Analysis [PDF]

open access: yesFrontiers in Medicine, 2021
Objectives: Retinal nerve fiber layer (RNFL) thickness has been detected by numerous studies about alterations and abnormalities in childhood glaucoma, but these studies have yielded inconsistent results about the RNFL thinning region.
Yuwen Wen, Yingting Zhu, Yehong Zhuo
doaj   +2 more sources

A Case of Refractory Childhood Glaucoma Associated With Sturge–Weber Syndrome Treated With Baerveldt Glaucoma Implant [PDF]

open access: yesCase Reports in Ophthalmological Medicine
We reported the clinical course of refractory childhood glaucoma associated with Sturge–Weber syndrome (SWS) treated with Baerveldt glaucoma implant (BGI). The patient was a 14-year-old male diagnosed with SWS after birth.
Wakako Imamura   +8 more
doaj   +2 more sources

Glaucoma in Childhood

open access: yesDelhi Journal of Ophthalmology, 2014
Glaucoma in childhood is a potentially blinding condition, yet, there is a lack of epidemiologic and clinical data regarding this pathology. Unlike glaucoma in adults, which is notoriously difficult to detect since there are no symptoms, glaucoma in ...
Savleen Kaur   +2 more
doaj   +3 more sources

Genetic changes and testing associated with childhood glaucoma: A systematic review. [PDF]

open access: yesPLoS ONE
Many forms of childhood glaucoma have been associated with underlying genetic changes, and variants in many genes have been described. Currently, testing is variable as there are no widely accepted guidelines for testing.
Anika Kumar, Ying Han, Julius T Oatts
doaj   +2 more sources

Study of corneal biomechanical properties in patients with childhood glaucoma [PDF]

open access: yesInternational Journal of Ophthalmology, 2020
AIM: To study of corneal biomechanical properties and intraocular pressure (IOP) measured with Corvis Scheimpflug Technology (ST) in patients with childhood glaucoma (CG). METHODS: Cross-sectional study in which 89 eyes were included 56 of them with CG.
Sara Garcia Caride   +3 more
doaj   +2 more sources

Reversible cupping and persistent vessel narrowing after glaucoma surgery in childhood glaucoma: a quantitative fundus photograph study [PDF]

open access: yesFrontiers in Medicine
PurposeTo investigate postoperative changes in peripapillary retinal vessel caliber and optic disc structure in childhood glaucoma.DesignProspective, comparative cohort study with a 2-year follow-up.MethodsThis study included 24 glaucomatous eyes ...
Miao Zhang   +5 more
doaj   +2 more sources

Childhood glaucoma – A review of basics

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth, 2022
Childhood glaucoma is a rare disease associated with significant pressure related visual loss and ocular comorbidity. It consists of a heterogeneous group of diseases which can be classified based on etiopathogenesis and morphology.
Sucheta Parija, Saswati Sen
doaj   +2 more sources

Genetic Basis of Non-Syndromic Childhood Glaucoma Associated with Anterior Segment Dysgenesis: A Narrative Review [PDF]

open access: yesPharmaceuticals
Twenty causative genes have been reported that cause non-syndromic childhood glaucoma associated with anterior segment dysgenesis. FOXC1, PAX6 and PITX2 are the most well-known, but cases linked to SLC4A11, PITX3 and SOX11 have also been reported.
Nicola Cronbach   +2 more
doaj   +2 more sources

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