Pediatric

In a small case series of 20 padeiatric cataract patients(includes single and both eyes).

To identify the types of Waardenburg syndrome, especially type 4 or Shah Waardenburg syndrome as it has the highest mortality

There are many different causes for corneal clouding/opacification which include both local ophthalmic causes as well as systemic causes. Mucopolysaccharidosis is a rare cause. So we present a case of Mucopolysaccharidosis Type IV, who presented with bilateral corneal clouding and other systemic features of this storage disorder.

To determine the amount of myopic shift in children after cataract surgery with IOL implantation and to evaluate success in achieving the target refraction

Developmental anomaly causing bilobed lens with anterior segment dysgenesis is an extremely rare condition.

Congenital corneal staphyloma is rare congenital disorder with keratinized,ectatic cornea protruding anteriorly.Presence of systemic features(cleft palate & VSD)facilitated in it being diagnosed as a clinical variant of Peters anomaly.

Choristoma of the eye are common epibulbar and ocular tumours in children, but osseous choristoma of the eye are very rare with few case reports being published in literature. We report one such case.

To describe case of aniridia with ptosis, lens coloboma, myopia & foveal hypoplasia.

To compare the Macular And Retinal Nerve Fiber Layer Thickness in Amblyopic And Normal Children Of 5-18 Age Group ”

To compare the efficacy and compliance with smart eye glasses and conventional patching in management of Unilateral Refractive Amblyopia.

To report the clinical profile and outcomes of lensectomy with anterior vitrectomy in a series of children with ectopia lentis

To evaluate the ophthalmic manifestation of orbital metastasis due to neuroblastoma

Two days old girl baby born to 2nd degree consanguineously married parent, delivered by emergency LSCS was presented with parchment like skin lesion all over the body.

Refractive error often goes undetected in children as there is no provision mandatory vision testing. This is an important cause of amblyopia.

To report a case of successful correction of head position and effective vision improvement in case of congenital nystagmus after modified Anderson operation.

To assess the feasibility and complications associated with IOL implantation in pediatric traumatic cataract

A 3 month-old female presented with bilateral corneal opacity associated with mucopurulent discharge for last one and a half months.

We present the case of a 10 year old child with Weill-Marchesani syndrome. The clinical diagnosis was made on the basis of the characteristic musculoskeletal features like short stature, broad head, expressionless facies, hypoplastic maxilla, shallow orbits, misaligned teeth and ocular manifestations including bilateral microspherophakia and progressive lenticular myopia.

To do the detailed eye examination in global developmental delay and cerebral palsy children for refractive error and other eye problems for better visual rehabilitation.

A male child aged 20 years presented with complain of diminution of vision in right eye since childhood.

A retrospective review of all the patients presenting to pediatric ophthalmology clinic with congenital nasolacrimal duct obstruction between Jan 2005 and June 2013 were reviewed to identify those who also had amblyopia risk factors.

This prospective interventional study included uncooperative children aged 1-16 years without acute medical condition but normal cardio respiratory status.

A seven day old neonate,1.8kg weight,gestational age 34 weeks,was examined on receiving a bedside call from neonatal ICU for some yellowish matter coming out of left eye(LE).

The studies comparing axial lengths in unilateral cataracts have showed contrasting results.

Fraser syndrome is a rare autosomal recessive (AR) disorder with cryptophthalmos, laryngeal, genitourinary ,craniofacial and musculoskeletal anomalies, orofacial clefting ,and mental retardation.

Prospective study of 59 children (< 15 years) with amblyopia was done between Jan to Dec 2015.

Reporting a 14 year old male child who presented with defective vision in both eyes since childhood.

In this presentations, authors share their experience of Toric and Multifocal Toric IOLs in Pediatric Cataract Cases.

To narrow the differential diagnosis and establish the role of ophthalmic ultrasonography in leukocoria.

Crouzon syndrome accounts for about 4.8% of all cases of craniosynostosis and occurs in approximately 1.6 per 100,000 live births worldwide.