A5007182715- Intraocular Surgery and Lenses
- Retinopathy of Prematurity Studies
- Ocular Oncology and Treatments
- Neonatal and fetal brain pathology
- Healthcare Systems and Public Health
- Neurological diseases and metabolism
- Retinal and Optic Conditions
- Human Health and Disease
- Ocular Diseases and Behçet’s Syndrome
- Retinal Development and Disorders
- Ophthalmology and Eye Disorders
- Nonmelanoma Skin Cancer Studies
- Pediatric Urology and Nephrology Studies
- Cerebral Venous Sinus Thrombosis
- Neurological Complications and Syndromes
- Retinal and Macular Surgery
- Hematopoietic Stem Cell Transplantation
Medical University of Sofia
2021
Alexandrovska Hospital
2017-2020
The travel distance from home to a treatment centre, which may impact the stage at diagnosis, has not been investigated for retinoblastoma, most common childhood eye cancer. We aimed investigate burden and its on clinical presentation in large sample of patients with retinoblastoma Africa Europe.A cross-sectional analysis including 518 treatment-naïve residing 40 European countries 1024 43 African countries.Capture rate was 42.2% expected 108.8% Europe. were older (95% CI -12.4 -5.4,...
Introduction. A dramatic increase of myopia worldwide has been observed in recent years. New risk factors for the development have target numerous investigations. The basis our research is correlation between serum levels vitamin D [25(OH)D] and itself. Purpose: To find out relationship 25(OH) myopia. Patients methods: study included 222 children with different refraction status. Full ophthalmologic examination, cycloplegic refraction, echobiometry were performed. 25(OH)D measured by liquid...
Миелинизираните ретинални нервни влакна (МРНВ) или т.нар. fibrae medullaris retinae са рядка конгенитална аномалия. Най-често се наблюдават като изолирана очна находка, обикновено протичаща асимптомно, диагностицираща случайно при преглед по друг повод. Могат да и част от рядък синдром, характеризиращ с наличието на ипсилатерална МРНВ, аксиална миопия амблиопия - триадата Straatsma. Представяме три клинични случая този конгенитален синдром.
Фамилната ексудативна витреоретинопатия (ФЕВР) е рядко генетично и клинично хетерогенно заболяване, дължащо се на нарушен процес съдова диференциация, водещо до непълна васкуларизация ретината. ФЕВР определя като състояние, наподобяващо ретинопатия недоносеното, но с изразена фамилна предиспозиция при липсата анамнеза за преждевременно раждане и/или кислородотерапия. Характерна е, както асиметрията патологичния в двете очи един същи пациент, така голямата вариабилност симптомите членовете...
Introduction: Determination of the scope surgical interventions, either retropositioning or myectomies horizontal rectus extraocular muscles is based on calculations that do not take into account distance insertion respective muscle. Aim : The aim this article to assess variations muscles. Materials and M ethods: research includes 63 children (126 eyes) with an average age 4 years months (the youngest 1y 2m old; oldest 16y old) comitant strabismus, all whom underwent surgery for a period 2...
Coats disease is a rare, in about 90% of cases unilateral idiopathic eye pathology. It characterized by telangiectatic and aneurysmally altered retinal blood vessels progressive intra- subretinal exudation, which can lead to exudative detachment. Most often the symptoms manifest advanced stages. Purpose: To report case with disease. 10 year old boy, admitted Eye Clinic University Alexandrovska Hospital – Sofia, leucocoria strabismus right eye. Method: Full ophthalmic orthoptic examination,...