VKH can present in elderly. immunomodulator is highly recommended in senior to prevent side effect of steroid along with recurrence of infection.VKH can present in elderly. immunomodulator should be considered in senior to prevent side effects of steroid along with recurrence of infection. Pigment dispersion Syndrome (PDS) is a disorder with a beginning in mid-twenties. There happens a disturbance associated with iris pigment epithelium and deposition of pigment granules through the entire anterior portion. The incidence of PDS is 4-8/ 100,000. This disorder is much more commonly observed in Caucasians and is regarded as being unusual in Indians. A 33-year-old male served with the grievance of headache for 90 days. He previously typical sight both in eyes with visual acuity of 6/6. Krukenberg’s spindle, a classic indication of pigment dispersion syndrome ended up being evident on slit-lamp examination throughout the posterior corneal surface. Gonioscopy revealed a heavy and uniformly pigmented trabecular meshwork. OCT (Optical Coherence Tomography) demonstrated a characteristic iris configuration in the form of a mid-peripheral posterior bowing of this iris .Retinal neurological fibre level evaluation done on OCT disclosed glaucomatous thinning when you look at the right eye and a far more advanced problem in the left attention. A visual area evaluation unveiled the area to be outside normal limits in both the eyes pointing towards an analysis of pigment dispersion glaucoma. The objective of showing this case is to caution the clinicians to very carefully examine youthful emmetropes which present with Krukenberg’s spindle since it could be involving PDS. Clients with Krukenberg’s spindle and without elevated lOP in many cases are treated as regular. These clients should be cautioned regarding feasible future effects associated with condition and counseled about the hereditary nature associated with problem.The purpose of presenting this case is to caution the physicians to very carefully examine young emmetropes which provide with Krukenberg’s spindle because it could possibly be involving PDS. Customers with Krukenberg’s spindle and without elevated lOP in many cases are addressed as normal. These clients must be cautioned regarding possible future consequences for the disease and counseled concerning the genetic nature of the problem. Progeria also known as Hutchinson Gilford Progeria Syndrome (HGPS) (MIM176670) is a very unusual fatal hereditary untimely aging problem. It is characterized by retarded physical development, accelerated degeneration of your skin, aerobic and musculoskeletal abnormalities. Other features include prominent eyes, slim nostrils, little chin and slim lips. Eyebrow hair loss, madarosis and lagopththalmos are the common ocular manifestations. We report an incident of five yr old man with grievances of vexation in brilliant light and a whitish look inside the correct eye for 2 months. He was associated with the moms and dads. They complained of loss in lashes and eyebrows. Within the developmental history he had been regular at birth till the age of twelve months then they noticed steady hair fall, delayed growth, wrinkling of skin, rise in measurements of mind and thinning of limbs. Ocular cysticercosis is a preventable reason behind loss of sight. It is caused by parasitic infestation due to the larval type of Taenia solium. Bad sanitation and incorrect handling of meals and beef items are the most important causes for cysticercosis infestation. Two instances of myocysticercosis presented to the medical center differently. A 12 years man, first instance given drooping of correct eye (RE) upper top with recurrent swelling, discomfort, redness with moderate annoyance and periodic nausea for 1 and half months. On assessment inflammation of RE top lid, moderate ptosis, abaxial proptosis with limited motility in upgaze was noted. Orbital CT (computer system tomography) scan and ocular ultrasound reports revealed findings suggestive of myocysticercosis of superior rectus muscle of RE. Routine microscopic examination (RME) of stool demonstrated eggs of Taenia. Complete bloodstream count (CBC) revealed eosinophilia. As a suspected case of myocysticercosis and because the in-patient lived at an endemic zone, empirical treatment with albeae. Both the clients enhanced well with no recurrence until last visit 17 months in 12 many years son and six months in 55 many years male and after that he destroyed to check out. Myocysticercosis may appear at any age. There clearly was equal need for clinical, radiological, microbiological and histopathological assistance for proper diagnosis and management of cysticercosis. Health therapy along side surgical excision for the cyst with it’s content may be required within the management of myocysticersosis.Myocysticercosis may appear sports and exercise medicine at all ages. There is equal significance of medical, radiological, microbiological and histopathological assistance for proper analysis and management of cysticercosis. Health therapy along with surgical excision of the cyst with it’s content may be required when you look at the management of myocysticersosis. Perfurocarbon Liquid (PFCL) is an essential adjunct of retinal detachment surgery. Subfoveal migration of PFCL is an uncommon and sight threatening complication of the use. Different practices have already been explained because of its reduction. But, no consensus on ideal technique of its removal is founded.