purpose : to evaluate the visual results of amblyopic therapy in pediatric patients with monocular abnormalities. methods : the hospital records of visually immature patients with unilateral organic ocular abnormalities and decreased visual acuity, who presented to the pediatric ophthalmology clinic over a one year period, were reviewed. those who had 8 years old of age or less and underwent am...

Introduction: Chronic renal disease compromises of several renal involvements and several causative risk factors such as debates mellitus, hypertension, and old age. Ocular involvement seems to be related to chronic renal failure and hemodialysis as indicated by different studies. The aim of this study was the evaluation of prevalence of ocular manifestation in hemodialysis patients of Hamadan ...

PURPOSE To determine the frequency of cerebellar and cerebral abnormalities on brain imaging studies in children with congenital ocular motor apraxia. METHODS Brain imaging studies were performed in 19 children with typical congenital ocular motor apraxia who were in the care of a visual impairment program at a children's hospital. Independent clinical review categorized the subjects as havin...

Abstract Introduction: The aim of this study was to clinically evaluate lid margin abnormality, meibomian glands expression and tear function changes in patients with primary pterygium. Methods: Fifty normal 50 pterygia participants without other ocular pathologies were randomly selected from who attended an ophthalmology visit. gland expression, break-up time, Schirmer's test results surface d...

Haematological diseases encompass a wide spectrum of disorders that can present with ocular manifestations. Indeed, ocular manifestations may be the initial indication of an underlying haematological disorder. Blood disorders are one of the major health problems presenting with variable clinical manifestations. Nutritional anemia remains the common haematological abnormality especially in third...

BACKGROUND Recent studies have demonstrated that pterygium has a close relationship with dry eye disease. This study is to determine abnormalities in meibomian gland and tear function in patients with pterygium and to assess the relationship between the variables. MATERIALS AND METHODS Forty eyes from forty patients with primary nasal pterygium and forty eyes from forty volunteers without ocu...

Goldenhar syndrome is a developmental abnormality of 1st & 2nd branchial arch involving the craniofacial microsomia with ocular & vertebral abnormality. Though most of the cases are sporadic, some familial association is also found in autosomal dominant or recessive manner. Teratogenic effect of some toxic substances may lead to the condition. Ocular abnormalities are epibulbar dermoid, lipoder...

BACKGROUND Wilson's disease is an autosomal recessive genetic disorder resulting from an abnormality of copper metabolism. The excessive accumulation of copper in the brain induces an extrapyramidal syndrome. Oculomotor abnormalities occur in most extrapyramidal disorders but have rarely been studied in Wilson's disease. OBJECTIVE To evaluate the ocular motility manifestations of Wilson's dis...