Results 91 to 100 of about 356,068 (177)
Congenital glaucoma, a complex and diverse condition, presents considerable difficulties in its identification and categorization. This research used Next Generation Sequencing (NGS) whole-exome data to create a categorization framework using machine ...
Muhammad Iqbal +6 more
doaj +1 more source
OBJECTIVE:This meta-analysis aims to evaluate the incidence of secondary glaucoma in patients under the age of 2 years who underwent congenital cataract surgery with or without primary intraocular lens (IOL) implantation. METHODS:An electronic literature
Shuo Zhang +5 more
doaj +1 more source
Comparison between biometry of X-linked megalocornea and congenital glaucoma.
(A) AC, anterior chamber depth (back of cornea to front of lens); AL, axial length (anterior corneal surface to vitreo-retinal interface at the back of the macular).
Pirro G. Hysi (110207) +22 more
core +1 more source
Mutations in the OCRL1 gene result in the oculocerebrorenal syndrome of Lowe, with symptoms including congenital bilateral cataracts, glaucoma, renal failure, and neurological impairments.
Emilie Song +8 more
doaj +1 more source
Primary congenital glaucoma in Vietnam: analysis and identification of novel CYP1B1 variants
Primary congenital glaucoma in Vietnam: analysis and identification of novel CYP1B1 ...
Huy Thinh Tran (6760715) +10 more
core +1 more source
Clinical characteristics of patients with pediatric glaucoma treated at the Santander Ophthalmology Foundation Clínica Carlos Ardila Lülle [PDF]
ResumenObjetivo: Caracterizar los pacientes atendidos por glaucoma pediátrico, identificar el tratamiento más utilizado para cada subgrupo y conocer los resultados en referencia al control de la presión intraocular. Método: Estudio retrospectivo mediante
Fuentes, Vanessa C. +1 more
core
CYP1B1 mutational screening in a Portuguese cohort of primary congenital glaucoma patients
CYP1B1 mutational screening in a Portuguese cohort of primary congenital glaucoma ...
M. J. Simões (2820919) +6 more
core +1 more source
FOXC2, PITX2 and CYP1B1 variants identified in congenital glaucoma patients.
FOXC2, PITX2 and CYP1B1 variants identified in congenital glaucoma patients.
Susana Alexandre-Moreno (6243632) +7 more
core +1 more source
.“ Confocal Microscopy in the study of primary congenital glaucoma”.
Study of the Corneal Modifications in the primary congenital glaucoma evalueted by Confocal ...
L. COLELLA +5 more
core
Brain MRI findings in infants with primary congenital glaucoma
Background: Congenital glaucoma appears in the first months of life, eventually at birth. Isolated congenital glaucoma is characterized by minor malformations of the irido-corneal angle of the anterior chamber of the eye. Clinical manifestations include
Dai Alper, Saygili Oguzhan
doaj

