Horner syndrome is a combination of signs and symptoms brought on by the disruption of a nerve path from the brain to the face and eye on one side of the body. Typically, Horner syndrome leads to a decreased student dimension, a sagging eyelid and decreased sweating on the affected side of your face. Horner syndrome is the outcome of another medical issue, such as a stroke, tumor or spinal cord injury. In some cases, no underlying cause can be found. There's no specific therapy for Horner syndrome, but treatment for the underlying cause might recover normal nerve function. Horner syndrome is additionally understood as Horner-Bernard syndrome or oculosympathetic palsy. Symptoms and signs, especially ptosis and anhidrosis, may be hard and subtle to identify. In people with Horner syndrome that happens before the age of 2, the colored part of the eyes may differ in color, with the iris of the affected eye being lighter in shade than that of the untouched eye. People that develop Horner syndrome after age 2 do not generally have iris heterochromia. The irregularities in the eye area pertaining to Horner syndrome do not generally affect vision or health and wellness. The nerve damages that causes Horner syndrome may result from other wellness troubles, some of which can be dangerous. Children who get Horner syndrome before age 2 also can have: One iris, the colored circle the student, that's a lighter color than the other; A lack of flushing on one side of their face on hot days or after playing. One of three pathways may be associated with Horner syndrome: This path entails the nerves that range from the hypothalamus in your brain to your chest, with your brain stem and spinal cord. Only 5% of people who have Horner syndrome are birthed with it.
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