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1.
Indian J Ophthalmol ; 65(9): 818-825, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28905824

ABSTRACT

PURPOSE: To analyze the current practice patterns of Indian pediatric ophthalmologists in the management of lens anomalies. This study was conducted in a tertiary eye care hospital and involved an online questionnaire survey for practicing pediatric ophthalmologists in India. METHODS: A questionnaire was devised by the authors, which included the various options available for the management of lens anomalies in children. The questionnaire was sent to each of them using an online portal. Commercial software (Stata ver. 13.1; StataCorp, College Station, TX, USA) was used for statistical analysis. RESULTS: In unilateral cataracts in children aged <6 months, 85.42% of surgeons did not prefer to insert an intraocular lens (IOL). In the age group of 6-12 months, almost half of them preferred to insert an IOL. In the age group of 12-24 months and> 24 months, 92.63% and 88.54%, respectively, preferred to insert an IOL. In bilateral cataracts, in children aged <6 months, 91.84% of surgeons did not prefer to insert an IOL, whereas in the age group of 6-12 months, 69.39% did not prefer to insert an IOL. In the age group of 12-24 months and> 24 months, 80.61% and 90.82%, respectively, preferred to insert an IOL. Seventy-four percent of surgeons preferred to use a single-piece hydrophobic acrylic IOL. CONCLUSION: The management of lens anomalies by pediatric ophthalmologists in India varies with laterality and appears to be comparable to that followed worldwide.


Subject(s)
Cataract/complications , Ectopia Lentis/surgery , Lens, Crystalline/abnormalities , Ophthalmologists/standards , Phacoemulsification/methods , Practice Patterns, Physicians' , Cataract/congenital , Cataract/epidemiology , Child, Preschool , Ectopia Lentis/complications , Ectopia Lentis/epidemiology , Female , Humans , India/epidemiology , Infant , Lens, Crystalline/surgery , Male , Prevalence , Surveys and Questionnaires
2.
Indian J Ophthalmol ; 64(6): 469-71, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27488160

ABSTRACT

Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is a rare autosomal dominant genetic disease. It is clinically characterized by four major features; blepharophimosis, ptosis, epicanthus inversus, and telecanthus. We report a case of a 1-year-old female with BPES with unilateral anterior persistent fetal vasculature (PFV). On examination, she was found to have all the clinical features of BPES, along with calcified and partially absorbed cataract with elongated ciliary processes in her left eye. B-scan of left eye showed attached retina with no evidence of posterior PFV. Systemic examination was normal. She underwent cataract surgery with primary posterior capsulotomy with intraocular lens implantation under general anesthesia. Literature search did not reveal any previous reports of unilateral anterior PFV and BPES. The clinical features, other associations, and the difficulties in the surgical management of this condition are discussed.


Subject(s)
Blepharophimosis/surgery , Persistent Fetal Circulation Syndrome/surgery , Posterior Capsulotomy/methods , Skin Abnormalities/surgery , Urogenital Abnormalities/surgery , Vitrectomy/methods , Blepharophimosis/diagnosis , Female , Humans , Infant , Persistent Fetal Circulation Syndrome/diagnosis , Skin Abnormalities/diagnosis , Urogenital Abnormalities/diagnosis
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