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Anisocoria and Horner's Syndrome
Anisocoria is a condition where one pupil is larger than the other. You can be born with anisocoria or develop it later in life.
Several factors can cause anisocoria, including Horner's syndrome. In this case, an underlying medical condition may be diagnosed by the doctor. This article looks at Horner's syndrome and its relationship to anisocoria.
What is Horner's syndrome?
Horner's syndrome, also known as Horner-Bernard syndrome or oculosympathetic palsy is a rare disorder resulting from nerve damage. The symptoms of Horner's syndrome include a drooping upper eyelid, unequal pupil sizes and a constricted pupil on the affected side. People with congenital Horner's syndrome often have a lighter coloured iris of the eye on the affected side compared to the iris of the eye on the unaffected side.
Horner's syndrome is the result of a disrupted nerve pathway from the brain to the face and the eye on one side of the body. The underlying causes for this vary and, in some cases, an underlying cause cannot be found.
Congenital Horner's syndrome is when the condition is passed down through families and is present from birth. Acquired Horner's syndrome appears after the newborn period. Both are the result of damage to the sympathetic nervous system.
Can Horner’s syndrome affect both eyes?
Horner's syndrome typically affects one side of the face, affecting only one eye. It does not usually cause problems with a person's vision.
How is Horner’s syndrome related to anisocoria?
The sympathetic nerves are responsible for dilating the pupil and raising the eyelid. Horner's syndrome is caused when these nerves are damaged.
Damaged sympathetic nerves cause the pupil in the eye on the affected side to become smaller compared to the eye on the unaffected side. The affected eye also has problems dilating. When the pupils in both eyes are different sizes at the same time, this is known as anisocoria.
Horner’s syndrome symptoms and causes
Signs and symptoms associated with Horner's syndrome usually only affect one side of the face.
What are the three classic signs of Horner's syndrome?
The three classic signs of Horner's syndrome are:
- A constricted pupil (miosis)
- Drooping of the upper eyelid (ptosis)
- Reduced sweating or no sweating on the whole side of the face or a patch on the affected side of the face (anhidrosis)
Other symptoms of Horner's syndrome include:
- A sunken appearance to the eye (enophthalmos)
- A difference in pupil size (anisocoria)
- Delayed pupil dilation or little pupil dilation in dim light
- A slight elevation of the lower lid
Children with Horner’s syndrome might have additional signs and symptoms, including:
- A lighter iris colour in the affected eye
- Lack of flushing (on the affected side) as a result of heat, emotional reactions or physical exertion
Causes of Horner’s syndrome
Horner's syndrome is a result of nerve damage from injury, compression or disease. Causes include:
- Neck or shoulder injury during birth
- A stroke in the brainstem
- Trauma to the neck, chest or upper spinal cord (or surgery involving them)
- Lung cancer
- Damage to the aorta
The cause of Horner’s syndrome is not always identifiable. These cases are known as idiopathic Horner syndrome.
Does Horner's syndrome cause pain?
Horner's syndrome can cause sudden neck pain and headaches. These are more severe symptoms of Horner's syndrome. Other serious symptoms include feeling dizzy, trouble seeing and weak muscles or lack of control over muscle movements.
What nerve is damaged in Horner's syndrome?
The nerve that is damaged in Horner's syndrome is the oculomotor nerve and is part of the sympathetic nervous system. The sympathetic nervous system regulates the functions that enable you to respond to changes in your environment. It is sometimes referred to as your body's 'fight or flight' response.
The oculosympathetic pathway is responsible for sending messages from the brain to the eye. The signals in this pathway send messages to your body so that it can respond to stress.
Does Horner’s syndrome go away?
Horner's syndrome often goes away when the underlying cause is treated effectively. Effective treatment of the underlying cause can restore nerve function.
What can be done for Horner's syndrome?
Nothing can be done for Horner's syndrome until the underlying cause is diagnosed. Treatment then depends on this underlying cause and might include:
- Surgery, chemotherapy or radiation (for cancer)
- Antibiotics for infectious diseases
- Anti-inflammatory drugs
- Clot-dissolving agents (for certain strokes)
- Minimally invasive treatments (for carotid artery dissection)
Diagnosis of Horner's syndrome
Diagnosing Horner's syndrome can be challenging as there are many other medical conditions which have the same symptoms, such as a dilated pupil or a drooping eyelid. Other conditions with these symptoms include optic neuritis and third nerve palsy.
Those with anisocoria should consider getting a diagnosis for Horner's syndrome. A dilation lag of the smaller pupil will help determine if one has Horner's syndrome. It also helps to distinguish the symptoms from physiologic anisocoria.
Sometimes the underlying cause of Horner's syndrome is harmless; however, other times, it can be life-threatening, for example, lung cancer, carotid artery dissection or neuroblastoma.
A detailed account of medical history and a physical exam are essential for the diagnosis of Horner's syndrome. A doctor will ask questions about the symptoms to try and decipher the underlying cause. They will also ask questions to see if Horner’s syndrome is the result of medication or injury from a medical procedure.
Patients with Horner's syndrome will also undergo an eye exam. During the exam, the doctor will look at their pupillary dilator muscle by seeing how their pupils respond to light and dark. The eye exam will also check eye movement.
Pharmacologic tests are sometimes used in the diagnosis of Horner's syndrome. This includes using apraclonidine eye drops or cocaine to see how your eye responds. Apraclonidine in the diagnosis will cause pupillary dilation in the affected pupil.
Blood and laboratory tests may also be required in the diagnosis of Horner's syndrome.