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Authors present ophthalmological findings in male patient, which was examined because of total bilateral congenital cataract at the age of 4, 5 months. Patient was registered by a neurologist because of central hypotonia and mental retardation. Complex examination suspected Lowe syndrome. Diagnosis of Lowe syndrome was established by metabolic examination and genetic tests. By genetic examination ...

Authors present ocular findings in the patient send to Pediatric Ophthalmology department Childrens Univerity Hospital in Bratislava at the age of 3 years with congenital glaucoma on her right eye and high myopia bilateral. In family history short stature, myopia, facial dysmorfism and cataract occured. Mother of our patient suffered of myopia, her brother underwent surgery because of cataract, gr...

Aim: Case report of choroidal neovascularization (CNV) detection in patient who was treated for bilateral retinoblastoma in early childhood. Material and methods: Patient at 1.5 years of age treated for endophytic retinoblastoma stage 4 (according to the Reese-Ellsworth classification) bilaterally, with a positive mutation in the Rb1 gene. After undergoing bilateral retinal laser treatment and 6 c...

Aim: To introduce the topic of pediatric keratoconus, highlighting the importance of routine corneal topography and tomography in children and adolescents from predisposed groups. To attempt to ensure the early detection of keratoconus and its subclinical form, enabling early treatment, which brings better expected postoperative results. Material and methods: Using the corneal tomograph Pentacam A...

Aim: To clarify the possibilities and role of posterior segment imaging in patients with neurofibromatosis type I (NF1), and to show the prevalence of this disease in the pediatric population in Slovakia. Material and methods: Until recently, ophthalmologic consultations in patients with NF1 were limited mainly to the observation of Lisch nodules of the iris and the presence of optic nerve glioma....