Eye diseases

Syndrome of vascular dysregulation

medical condition

medical condition

medical condition

common and highly contagious viral infection of the eye

Human disease

eye disease characterized by slit-like depigmented areas of the iris with up to 50% of patients going on to develop gluacoma

disease

medical condition

condition of pain in a lost eye

Corectopia is the displacement of the eye's pupil from its normal, central position. It may be associated with high myopia or ectopia lentis, among other conditions. Medical or surgical intervention may be indicated for the treatment of corectopia in some cases.

human disease

human disease

medical condition

a hypotrichosis that has material basis in a autosomal recessive mutation of CDH3 on chromosome 16q22.1.

medical condition

syndrome that is a chronic unilateral (or rarely bilateral) iridocyclitis appearing with the triad of heterochromia, predisposition to cataracts and glaucoma, and keratitic percipitates on the posterior corneal surface

Dacryocystocele (Dacryocystitis) or timo cyst is a benign, bluish-gray mass in the inferomedial canthus that develops within a few days or weeks after birth. The uncommon condition forms as a result as a consequence of narrowing or obstruction of the nasolacrimal duct, usually during prenatal development. Nasolacrimal duct obstruction disrupts the lacrimal drainage system, eventually creating a swelling cyst in the lacrimal sac area by the nasal cavity. The location of the cyst can cause respiratory dysfunction, compromising the airway. The obstruction ultimately leads to epiphora, an abundanc

thumb|Fundoscopy demonstrating age-related macular degeneration. A maculopathy is any pathological condition of the macula, an area at the centre of the retina that is associated with highly sensitive, accurate vision.

Pelopsia, a facet of Alice in Wonderland Syndrome (AIWS), is a vision perception disorder in which objects appear nearer than they actually are. Objects may also appear to be coming closer when they are not. Pelopsia and other conditions that fall under AIWS are usually temporary, which may justify the lack of research done on this subject. Pelopsia can be caused by psychoneurotic phenomena, changes in atmospheric clarity, or sometimes by wearing a corrective lens. AIWS is most common in children, with them accounting for 2/3 of documented cases. The most common way to treat this disorder is b

The absence or defect of controlled, voluntary, and purposeful eye movement

congenital hereditary deformity of the eye surface

human disease

symptom

Human disease

ocular form of the larva migrans syndrome that occurs when larvae invade the eye

A staphyloma is an abnormal protrusion of the uveal tissue through a weak point in the eyeball. The protrusion is generally black in colour, due to the inner layers of the eye. It occurs due to weakening of outer layer of eye (cornea or sclera) by an inflammatory or degenerative condition. It may be of five types, depending on the location on the eyeball (bulbus oculi).

Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment