Results 31 to 40 of about 5,069,987 (201)
PurposeTo assess long-time results of primary surgical treatment in children with glaucoma after congenital cataract surgery.MethodsA retrospective study of 37 eyes from 35 children with glaucoma after congenital cataract surgery, who underwent surgery ...
Alicja Strzalkowska +5 more
doaj +1 more source
Therapy of congenital glaucoma [PDF]
The primary therapy of all forms of primary and secondary congenital glaucoma is surgical. In the last few decades, the options for customized surgical approach to different types of childhood glaucoma have significantly developed.
Grehn, Franz, Hoffmann, Esther
core
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
Novel CYP1B1 mutations and a possible prognostic use for surgical management of congenital glaucoma [PDF]
AIM: To identify CYP1B1 gene mutations and evaluate their possible role as a prognostic factor for success rates in the surgical management of Egyptian congenital glaucoma patients.
Mohamed M. Khafagy +5 more
doaj +1 more source
Molecular genetics of primary congenital glaucoma [PDF]
Molecular genetic studies conducted during the last several years have thrown some light on the basic molecular defects in primary congenital glaucoma (PCG) and the rationale behind the clinical and genetic presentation of this paediatric eye condition.
M, Sarfarazi, I, Stoilov
openaire +2 more sources
POLYMORPHISM OF EYE DRAINAGE SYSTEM CHANGES IN GLAUCOMA
The study aim was to investigate structural peculiarities of sclera in different types of glaucoma, with an accent on changes of the eye drainage system. Materials and methods.
A. K. Lazareva +4 more
doaj +1 more source
Screening of West Siberian patients with primary congenital glaucoma for CYP1B1 gene mutations
Primary congenital glaucoma (PСG) is a visual organ pathology that leads to progressive blindness and poor vision in children. Its main cause is an anomaly of the anterior chamber angle.
D. E. Ivanoshchuk +6 more
doaj +1 more source
Ocular Manifestations of the Sturge–Weber Syndrome
Sturge–Weber syndrome (SWS) or encephalotrigeminal angiomatosis is a non-inherited congenital disorder characterized by neurologic, skin, and ocular abnormalities. A somatic activating mutation (R183Q) in the GNAQ gene during early embryogenesis has been
Kiana Hassanpour +4 more
doaj +1 more source
Corneal profile in primary congenital glaucoma [PDF]
AbstractPurposeTo investigate biomechanical and ultrastructural corneal parameters and ocular biometrics in the affected eyes of patients with unilateral primary congenital glaucoma (PCG) as compared to unaffected fellow eyes and age‐matched healthy controls.MethodsA total of 12 patients with treated unilateral PCG and 10 normal subjects were evaluated.
Azadeh, Doozandeh +6 more
openaire +2 more sources
Congenital glaucoma accompanied by natal teeth: A case report
Primary congenital glaucoma is a global problem, which is characterized by increased intraocular pressure and resulted in loss of vision if not timely and appropriately treated.
Yusuf Kale, Ümit Aksoy
doaj +1 more source

