Optico-Hemiplegic Syndrome

Opticohemiplegic syndrome (lat. syndromum opticum hemiplegicae; synonym: amaurotohemiplegic syndrome, opticopyramidal syndrome) –

most often developing on the surface of the brain and with pressure on it from another base, a disease in which weakening, plegia of both eye muscles, vision impairment (from the onset of amaurosis), headaches, gigranturia, neuritis occur with the maintenance of the integrity of peripheral and central neurons, garbage disposal for cerebellar disorders is one of them. Opticoplegic amaurosia syndrome in somatic and infectious diseases, which correspond to the symptoms of many diseases in the form of an intracranial tumor or some other cause. The basis is the severity of the pathological process at the fulcrum and disruption of contact between the brain and the external part, as a result of which numerous changes occur in this organ and the arteries adjacent to it.

Optico-hemiplegic syndrome syn., or amavrotoiko-hemioplegic (amibliotoic)-hypothalamic syndrome, is an anomaly of the optic nerve and the distal midbrain and predominantly damage to the pyramidal tract from the opposite abortive hemiplegia. **The syndrome spreads to one, less often to both, halves of the body.**

Optical hemiplegic syndrome is a brain lesion in which visual and sensory functions are impaired due to damage to certain areas of the cerebral cortex.

The left hemisphere is predominantly affected in relation to the healthy opposite zones. The disease occurs in young and middle-aged people. Symptoms are usually associated with damage to the left occipital lobe, subcortical nuclei, or frontal region. Often the patient complains of blurred vision and loss of sensation in the right half of the body. From ophthalmological