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  2. Volume 7, Issue 10
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Online ISSN: 2515-8260

Volume7, Issue10

Horner’s Syndrome – A Review

    Chandrakala B, Govindarajan Sumathy, Bhaskaran Sathyapriya

European Journal of Molecular & Clinical Medicine, 2020, Volume 7, Issue 10, Pages 531-535

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Abstract

Horner syndrome consists of unilateral ptosis, an ipsilateral miotic but normally reactive pupil, and in some cases, ipsilateral facial anhidrosis, all resulting from damage to the ipsilateral oculosympathetic pathway. Horner syndrome is also known as Horner-Bernard syndrome or Oculosympathetic palsy.It is a result of another medical problem, such as a stroke, tumor or spinal cord injury. In some cases, no underlying cause can be found. There's no specific treatment for Horner syndrome, but treatment for the underlying cause may restore normal nerve function. The nerves of the sympathetic trunk arise from the spinal cord in the chest, and from there ascend to the neck and face. The nerves are part of the sympathetic nervous system, a division of the autonomic (or involuntary) nervous system. Once the syndrome has been recognized, medical imaging and response to particular eye drops may be required to identify the location of the problem and the underlying cause
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(2020). Horner’s Syndrome – A Review. European Journal of Molecular & Clinical Medicine, 7(10), 531-535.
Chandrakala B, Govindarajan Sumathy, Bhaskaran Sathyapriya. "Horner’s Syndrome – A Review". European Journal of Molecular & Clinical Medicine, 7, 10, 2020, 531-535.
(2020). 'Horner’s Syndrome – A Review', European Journal of Molecular & Clinical Medicine, 7(10), pp. 531-535.
Horner’s Syndrome – A Review. European Journal of Molecular & Clinical Medicine, 2020; 7(10): 531-535.
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