Results 1 to 10 of about 1,904 (113)

Aniridia associated with congenital aphakia and secondary glaucoma

open access: yesIndian Journal of Ophthalmology, 2009
We report a case of aniridia associated with congenital aphakia and secondary glaucoma. A 35-year-old male presented with aniridia, congenital aphakia and secondary glaucoma in both eyes.
Rajul Parikh, Ravi Thomas
exaly   +4 more sources

Secondary developmental glaucoma in eyes with congenital aphakia [PDF]

open access: yesIndian Journal of Ophthalmology, 2022
Purpose: To describe the clinical spectrum and management of glaucoma in congenital aphakia. Methods: The demographics and clinical spectrum of eyes with congenital aphakia with and without glaucoma were compared, and management outcomes of congenital ...
Swathi Vallabh Badakere   +7 more
doaj   +2 more sources

Novel prenatally diagnosed compound heterozygous PXDN variants in fetal congenital primary aphakia and blepharophimosis

open access: yesTaiwanese Journal of Obstetrics and Gynecology, 2022
Objective: To precision survey a fetal congenital primary aphakia molecular etiology. Case report: A case of 42 years old pregnancy woman prenatal diagnostic examination by amniocentesis conducted at 17 weeks' gestation and demonstrated a normal female ...
Wei Shin Chou   +6 more
exaly   +3 more sources

A missing lens-congenital aphakia?

open access: yesKerala Journal of Ophthalmology, 2022
Congenital aphakia (CA) is a rare disease of the absence of the lens since birth. It may be primary or secondary. Primary aphakia is due to the failure of induction of surface ectoderm to form the lens.
Vidharthi Diwakaran   +2 more
doaj   +1 more source

Anterior segment alterations in congenital primary aphakia—a clinicopathologic report of five cases

open access: yesIndian Journal of Ophthalmology, 2020
Purpose: To report the clinicopathological features of corneal buttons in patients with congenital primary aphakia. Methods: Five corneal specimens of five patients with congenital primary aphakia who underwent penetrating keratoplasty (PKP) were studied
Sunita Chaurasia   +4 more
doaj   +1 more source

Genetics of the anterior segment dysgenesis

open access: yesTaiwan Journal of Ophthalmology, 2023
The anterior segment dysgeneses are a broad group of heterogeneous disorders characterized by developmental abnormalities of the anterior segment of the eye, including primary congenital aphakia, Peters sequence, aniridia, and Axenfeld–Rieger spectrum ...
Diego I Paredes   +3 more
doaj   +1 more source

Angle closure secondary to lens remnants in a patient with presumed aphakia: case report

open access: yesBMC Ophthalmology, 2022
Background Eyes with a short axial length or anterior chamber depth often develop narrowed anterior chamber angles in association with an enlarging crystalline lens.
Kristi Y. Wu   +2 more
doaj   +1 more source

Comparative analysis of anatomic parameters of the eyeball in children with ametropia, congenital glaucoma, aphakia and artiphakia

open access: yesРоссийский офтальмологический журнал, 2019
Purpose. To conduct a comparative analysis of the anatomical parameters of the eyeball in children with ametropia, congenital glaucoma, aphakia and artiphakia.Material and methods.
L. S. Khamraeva   +3 more
doaj   +1 more source

The Results of Morphometric Assessment of the Macular Zone in Congenital Cataract

open access: yesOftalʹmologiâ, 2018
Purpose: to study the morphological characteristics of the macular zone using optical coherence tomography to assess its development in congenital cataract. Patients and methods: a comprehensive ophthalmological examination was performed in 147 children (
L. A. Katargina   +3 more
doaj   +1 more source

Congenital cataract. Report 2. Current strategies of congenital cataract management in children: a review

open access: yesOftalʹmologiâ, 2014
Different approaches to surgical and pleoptic treatment of congenital cataract and amblyopia of obscure origin in children are represented. Main tendencies that determine the indications to surgical procedures and their terms are described.
N. Ya. Senchenko   +3 more
doaj   +3 more sources

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