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ULY CLINIC
ULY CLINIC
26 Septemba 2025, 01:01:53
Marcus Gunn’s phenomenon
Marcus Gunn’s phenomenon is a unilateral reflexive elevation of a ptotic upper eyelid that occurs during movement of the lower jaw, commonly observed in misdirectional cranial nerve syndromes. It reflects abnormal oculomotor (cranial nerve III) and trigeminal (cranial nerve V) interactions.
Pathophysiology
Normal physiology:
The levator palpebrae superioris elevates the upper eyelid under oculomotor nerve control.
The trigeminal nerve controls mastication muscles (masseter, temporalis) without influencing eyelid movement.
Abnormal physiology (misdirectional syndrome):
Aberrant reinnervation or misdirection of nerve fibers causes activation of the levator palpebrae superioris during mandibular movements.
Opening or lateral movement of the jaw triggers reflexive eyelid elevation, producing the characteristic jaw-winking appearance.
Associated findings: May coexist with congenital ptosis, amblyopia, or strabismus on the affected side.
Examination Technique
Patient positioning: Seated comfortably with the face visible.
Observation: Inspect for ptosis at rest and abnormal eyelid movement with jaw activity.
Jaw movements: Ask the patient to open the mouth and move the lower jaw side to side.
Documentation: Record laterality, degree of eyelid elevation, symmetry, and presence of ptosis.
Clinical Features
Feature | Manifestation |
Eyelid movement | Reflexive elevation of ptotic upper eyelid during jaw movement |
Ptosis | Present at rest on affected side |
Trigger | Mouth opening, jaw movement, lateral jaw motion |
Laterality | Usually unilateral |
Associated ocular findings | Strabismus, amblyopia, or congenital ptosis may co-occur |
Differential Diagnosis
Condition | Key Feature | Notes |
Marcus Gunn phenomenon | Jaw-winking ptosis, unilateral | Classic misdirectional syndrome |
Congenital ptosis | Persistent eyelid droop without jaw movement | No reflexive eyelid elevation |
Horner’s syndrome | Ptosis with miosis and anhidrosis | Sympathetic pathway lesion, no jaw-winking |
Myasthenia gravis | Variable ptosis, fatigable | Eyelid weakness improves with rest or ice test |
Mechanical ptosis | Eyelid droop due to mass or scarring | No reflexive movement |
Special populations
Children:
Commonly congenital; early recognition is important to prevent amblyopia and plan corrective surgery if needed.
Adults:
Rarely acquired; usually linked to trauma or aberrant reinnervation.
Limitations
Subtle jaw-winking may be missed if jaw movements are minimal.
Must differentiate from other causes of ptosis or eyelid retraction.
Requires careful observation and patient cooperation.
Patient counseling
Explain that jaw-winking occurs due to abnormal nerve wiring and is not harmful by itself.
Advise ophthalmology referral for assessment of vision, amblyopia risk, and surgical correction if indicated.
Reassure families that the phenomenon is usually congenital and isolated, but may need monitoring.
Conclusion
Marcus Gunn’s phenomenon is a clinical sign of misdirected oculomotor and trigeminal nerve activity, manifesting as reflexive elevation of a ptotic eyelid during jaw movement. Recognition is important for diagnosis, differentiation from other ptoses, and planning ophthalmologic management.
References
Marcus Gunn RM. Ptosis associated with winking of the eyelid on movement of the jaw. Br J Ophthalmol. 1883;67:377–380.
von Noorden GK, Campos EC. Binocular Vision and Ocular Motility: Theory and Management of Strabismus. 6th ed. St. Louis: Mosby; 2002.
Anderson RL, Baumgartner R. Congenital ptosis and Marcus Gunn jaw-winking phenomenon. Ophthalmology. 1991;98:96–101.
Wright KW. Pediatric Ophthalmology and Strabismus. 3rd ed. New York: Springer; 2012.
