1.9 Horner’s Syndrome (Oculosympathetic Palsy)

Date of last review:

22/6/2026

Date of next review:

22/6/2028

Date of publication:

17/8/2026


Differential diagnosis (1)

  • Mechanical causes of anisocoria or ptosis, including:  

    • Posterior synechiae 

    • Iris sphincter tears 

    • Surgical or traumatic iris injury 


Possible management by Optometrist

Advice (1) 

  • Take a thorough history, including:  

    • Use of new or topical medications affecting pupil size 

    • Associated visual, neurological, or systemic symptoms 

    • History of malignancy 

    • Recent head, neck, or facial trauma 

  • Review old photographs where physiological anisocoria is suspected 

  • Perform slit‑lamp examination to exclude mechanical causes 

  • Assess:  

    • Extraocular motility 

    • Presence and degree of ptosis 

Signs of Horner’s Syndrome 

  • Classically characterised by a triad of:  

    • Ipsilateral ptosis 

    • Miosis 

    • Anhidrosis 

  • All features are rarely present together 

  • Ptosis, when present, is typically mild (1–2 mm) and may be absent

  • Miosis is associated with a dilation lag, with anisocoria more evident in the dark 

  • Anhidrosis may involve the entire hemiface, a localised area, or be absent, depending on lesion location 

  • Onset very early in life may result in iris heterochromia 

Treatment (1) 

  • No treatment is required for this condition 


Typical dosage/duration 

(Blue text = IP, black text = non-IP)

  • Not applicable for this condition (7)  


Further management options (1) 

  • Immediate emergency referral is required if Horner’s syndrome is associated with neck pain  

    • This should be considered a neurological emergency, as it may indicate carotid artery dissection 

No referral normally required:  

  • Physiological anisocoria 

  • Tonic pupil 

  • Manage with reassurance and routine review as appropriate 


Possible management in secondary care or local/community pathways where available (1)

  • Investigation and management is often undertaken by a multidisciplinary team, depending on the underlying cause


College of Optometrists Clinical Management Guideline (1)  

Abnormalities of the pupil - College of Optometrists *

* With special thanks to The College of Optometrists for providing the evidence framework for diagnosis and management from the Clinical Management Guidelines (CMGs) for this condition. All references to the College/CMGs are included where appropriate and form the basis of the Community Eyecare Guidelines.


Guidance is informed by the following sources 

  1. College of Optometrists Clinical Management Guidelines Clinical Management Guidelines - College of Optometrists

  2. Advisory alignment with the College of Optometrists Formulary Optometrists' Formulary - College of Optometrists

  3. Advisory alignment with the BNF BNF (British National Formulary) | NICE

  4. Advisory alignment with the Summary Product Characteristics taken from the EMC Home - electronic medicines compendium (emc)

  5. Advisory alignment with Scottish Health Board formularies (where a clear majority is present) *

  6. Advisory alignment with expert consensus (CEGG), informed by sources 2-5 above

  7. Advisory alignment with expert consensus (CEGG) 

  8. “Annex C of the Statement” https://www.eyes.nhs.scot/for-professionals/legislation/

* Scottish formularies should be available within the Prescribing section of your Health Board pages on the eyes.nhs.scot website. If unavailable, contact your local Health Board for further information; Health Boards landing page 


If you have a query relating to this page, please email NSS.ComEyecareGuidelineGroup@nhs.scot