Retinoblastoma is the most common intraocular malignancy. Its incidence has been reported
to be 1 case in from 15 000 to 18 000 live births, or approximately 12, 6, or 4 cases per 1 …

Autosomal dominant North Carolina macular dystrophy (NCMD) is believed to represent a
failure of macular development. The disorder has been linked to two loci, MCDR1 (…

Inherited macular dystrophies (iMDs) are a group of genetic disorders, which affect the
central region of the retina. To investigate the genetic basis of iMDs, we used single-molecule …

Introduction: Intraocular lenses have always been a controversial topic in pediatric cataract
surgery. In the early 1990s in the post-Soviet states of Eastern Europe, intraocular lenses …

Background and objectives: primary congenital glaucoma (PCG) is a rare, potentially
blinding disease that affects children worldwide. The aim of the study was to describe the …

Background and Objectives: Danon disease is a multisystemic disorder associated with
variants in the LAMP2 gene, mainly affecting the cardiac muscle. Here, we report a …

Background and objective North Carolina macular dystrophy (NCMD) is a very rare autosomal
dominant hereditary disease. Up to date there are three types of NCMD described and …

Two siblings with ophthalmic findings, psychomotor retardation, somnolence, and seizures
underwent diagnostic studies, genetic investigations, ultrasonography, biomicroscopy, and …

Introduction: Since 1907, multiple transposition procedures have been established for the
treatment of abducens paralysis. The purpose of the study was to determine where the …

Introduction The use of Information and Communication Technology (ICT) for assessing and
treating cognitive and motor disorders is promoting home-based telerehabilitation. This …