A5080056326- Retinopathy of Prematurity Studies
- Neurological Disorders and Treatments
- Neonatal and fetal brain pathology
- Intraocular Surgery and Lenses
- melanin and skin pigmentation
- Retinal Development and Disorders
- Glaucoma and retinal disorders
- Connective tissue disorders research
- Retinal and Macular Surgery
- Neonatal Health and Biochemistry
- Ocular Disorders and Treatments
- Human Health and Disease
- Anesthesia and Neurotoxicity Research
Russian Children's Clinical Hospital
2020-2024
This article explains the necessity to clarify ideas about etiology and pathogenesis of amblyopia due accumulation information. Firstly, appearance new ophthalmological optometric instruments, it became possible detect distinct signs organic functional pathology various kinds in patients diagnosed with amblyopia, which were previously impossible detect. Secondly, modern highly effective informative neurophysiological methods vision process investigation allowed develop complete more adequate...
This article describes the definitions of amblyopia appearing in literature and discusses how exacly they reflect modern ideas about disease. Based on results analysis, it is recommended not to use widespread expression “lazy eye” as a synonym for amblyopia, since distorts essence this Two alternative ways searching correct definition are proposed. Key words: concept amblyopic component, lazy eye syndrome
Актуальность. Ретинопатия недоношенных (РН) — вазопролиферативное заболевание, приводящее к инвалидности по зрению. Цель. Выявление значимых факторов патогенеза пролиферативных стадий РН. Материал и методы. Прооперировано 2363 детей до 1 года (3415 глаз), исследована кровь у 173 (346 глаз). Мультивариантный анализ. Результаты. Снижение АТ III повышение D-димера активация свертывания крови, тромбодинамика: гиперкоагуляция в группе с РН гемофтальмом (63,0%). Наиболее низкие количества CD4 +...
This study investigated the prevalence and morphofunctional characteristics of retina in diagnosis various types Leber congenital amaurosis (LCA) among patients from Moscow region, based on data Consultative Diagnostic Center Morozov Children's City Clinical Hospital.
Achromatopsia (ACHM) is a rare autosomal recessive disease. Its mutation spectrum well described in other populations, but the data on ACHM prevalence and features Russia are insufficient. Purpose . To describe clinically genetically Russian cohort of AHCM for potential use targeted treatment approaches, including gene therapy. Material methods Out 18 patients with clinical manifestations ACHM, 10 were chosen (6 no kinship relatedness 4 relatedness) aged 12.3 ± 5.8 years. These underwent...
Persistent hyperplastic primary vitreous syndrome (PHPV) is a rare congenital anomaly associated with impaired regression of the embryonic vitreous. There still no unequivocal opinion on advisability and terms surgical treatment posterior form severe III IV stages PHPV. Objective. To determine optimal tactics for PHPV in children. Material methods. During 2017-2021 we examined performed intervention 18 children (18 eyes). The first group – under 2 years stage PHPV, second 1 year third from 3...