Horner's Reverse Syndrome

Horner's syndrome, also known as Horner's syndrome, is a rare and complex congenital disorder that causes atrophy of the facial and eye muscles, as well as abnormal pupillary function. This syndrome occurs when the cerebrospinal fluid or neurotransmitter needed to control eye movement moves too quickly to the eyeball, causing excessive

Horner Reverse Syndrome

Horner's inverse syndrome (lateral asymmetric abducens nerve palsy 3) is a classic neurological manifestation of a violation of the innervation of the extraocular muscles: the lateral rectus and oblique muscles. Identified in children with visual impairments. Disturbance of innervation is caused by the following reasons: congenital defects, intrauterine injuries, infectious diseases, brain tumors. The main diagnosis is an eye examination: comparing a unilateral motor defect of the oculomotor system with the other side, you can notice a restriction in the upward and inward movement of the eyeball. There is also a visual test based on the fact that the patient may have difficulty keeping his gaze in bright light and briefly (no more than a second) look at the light spot, due to impaired abduction of the eye due to involvement