Adie's pupil

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(Redirected from Adie's syndrome)

Adies pupil
Adies pupil

Other names[edit | edit source]

Holmes-Adie syndrome (HAS)

Introduction[edit | edit source]

Adie's pupil is a neurological disorder affecting the pupil of the eye and the autonomic nervous system.

Clinical features[edit | edit source]

It is characterized by one eye with a pupil that is larger than normal and constricts slowly in bright light (tonic pupil), along with the absence of deep tendon reflexes, usually in the Achilles tendon.

Pathophysiology[edit | edit source]

HAS is thought to be the result of a neurotrophic (acting on neurons, or nerve cells) viral infection that causes inflammation and damage to neurons in the ciliary ganglion, an area of the brain that controls eye movements, and the dorsal root ganglion, an area of the spinal cord involved in the response of the autonomic nervous system.

Progression[edit | edit source]

HAS begins gradually in one eye, and often progresses to involve the other eye.

Clinical features[edit | edit source]

At first, it may only cause the loss of deep tendon reflexes on one side of the body, but then progress to the other side. The eye and reflex symptoms may not appear at the same time. People with HAS may also sweat excessively, sometimes only on one side of the body.

Diagnosis[edit | edit source]

The combination of these 3 symptoms – abnormal pupil size, loss of deep tendon reflexes, and excessive sweating – is usually called Ross’s syndrome, although some doctors will still diagnose the condition as a variant of HAS.

Cardiovascular involvement[edit | edit source]

Some individuals will also have cardiovascular abnormalities.

Associated conditions[edit | edit source]

The HAS symptoms can appear on their own, or in association with other diseases of the nervous system, such as Sjogren’s syndrome or migraine.

Sex differences[edit | edit source]

It is most often seen in young women.

Inheritance[edit | edit source]

It is rarely an inherited condition.

Prognosis[edit | edit source]

  • Holmes-Adie syndrome is not life-threatening or disabling.
  • The loss of deep tendon reflexes is permanent.
  • Some symptoms of the disorder may progress.
  • For most individuals, pilocarpine drops and glasses will improve vision.

Treatment[edit | edit source]

  • Doctors may prescribe reading glasses to compensate for impaired vision in the affected eye, and pilocarpine drops to be applied 3 times daily to constrict the dilated pupil.
  • Thoracic sympathectomy, which severs the involved sympathetic nerve, is the definitive treatment for excessive sweating.
Adie's pupil Resources
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External links[edit | edit source]

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ICD codes[edit | edit source]

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Contributors: Prab R. Tumpati, MD