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Reactive arthritis. Rheumatoid arthritis. Ehlers-Danlos Syndrome. Sarcoidosis. Scleroderma. Systemic lupus erythematosus. Temporal arteritis. Relapsing polychondritis. Granulomatosis with polyangiitis 50-60% have ophthalmologic manifestations, which can be a presenting feature in a minority of patients.
Eye examination. Functional visual loss (FVL) also known as Functional vision loss or Nonorganic visual loss (NOVL) is a reduction in visual acuity or loss of visual field that has no physiological or organic basis. This disease can come under the spectrum of functional neurological disorder or somatic symptom disorder .
Chronic progressive external ophthalmoplegia ( CPEO) is a type of eye disorder characterized by slowly progressive inability to move the eyes and eyebrows. [ 1] It is often the only feature of mitochondrial disease, in which case the term CPEO may be given as the diagnosis. In other people suffering from mitochondrial disease, CPEO occurs as ...
Parinaud's syndrome is a constellation of neurological signs indicating injury to the dorsal midbrain. More specifically, compression of the vertical gaze center at the rostral interstitial nucleus of medial longitudinal fasciculus (riMLF). It is a group of abnormalities of eye movement and pupil dysfunction and is named for Henri Parinaud [6 ...
Individuals with nystagmus, Duane's retraction syndrome, 4th Nerve Palsy, and other eye movement disorders experience an improvement in their symptoms when they turn or tilt their head. Yoked prism can move the image away from primary gaze without the need for a constant head tilt or turn. Prism correction is measured in prism dioptres. A ...
Convergence insufficiencyis a sensory and neuromuscular anomaly of the binocular visionsystem, characterized by a reduced ability of the eyesto turn towards each other, or sustain convergence. Symptoms. [edit] The symptoms and signs associated with convergence insufficiency are related to prolonged, visually demanding, near-centered tasks. They ...
Metamorphopsia (from Greek: μεταμορφοψία, metamorphopsia, 'seeing mutated shapes') is a type of distorted vision in which a grid of straight lines appears wavy and parts of the grid may appear blank. People can first notice they suffer with the condition when looking at mini-blinds in their home. For example, straight lines might be ...
Muscle–eye–brain (MEB) disease, also known as muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A3 (MDDGA3), [2] is a kind of rare congenital muscular dystrophy (CMD), largely characterized by hypotonia at birth. Patients have muscular dystrophy, central nervous system abnormalities and ocular abnormalities.