Duane Syndrome Types

Duane Syndrome is classified into three types based on which eye movements are affected. The classification was developed by Huber in 1974 based on electromyographic studies.

Type 1 — Limited Abduction

Most common (~78% of cases)

What happens: The affected eye has significantly limited or absent ability to move outward (away from the nose). Movement inward (toward the nose) is normal or near-normal.

Globe retraction: When attempting to look inward, the eyeball retracts into the socket, and the eyelid opening narrows.

In daily life: People with Type 1 often develop a slight head turn toward the affected side to compensate, maintaining good binocular vision in their functional range.

Type 2 — Limited Adduction

Less common (~7% of cases)

What happens: The affected eye has limited ability to move inward (toward the nose). Outward movement is normal or near-normal.

Globe retraction: Retraction occurs when attempting to look inward, similar to Type 1.

In daily life: Head turns may be adopted to compensate. This type is sometimes confused with other forms of strabismus.

Type 3 — Limited Both Directions

Least common (~15% of cases)

What happens: The affected eye has limited movement in both directions — inward and outward.

Globe retraction: Retraction may occur when attempting to look in either direction.

In daily life: This type may present with a more notable head position. The degree of limitation can vary significantly.

Common Features Across All Types

  • Globe retraction: The hallmark feature. When the eye tries to adduct (look inward), the eyeball pulls back into the orbit.
  • Upshoot and downshoot: Abnormal vertical eye movements that occur during attempted adduction, caused by co-contraction of horizontal eye muscles.
  • Palpebral fissure narrowing: The eyelid opening becomes smaller during certain eye movements due to the globe retraction.
  • Compensatory head turn: A natural adaptation that allows maintaining binocular vision in the functional gaze range.

This information is for educational purposes. Consult an ophthalmologist for diagnosis and management.