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The undesirable wink.

Varsha Backiavathy1, Soham Pal1, Nisar Sonam Poonam1

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Summary
This summary is machine-generated.

Marin-Amat syndrome, a rare synkinesis after facial nerve palsy, causes involuntary eyelid closure with jaw movement. Management includes observation, botulinum toxin, or surgery, offering viable options for this condition.

Keywords:
Botulinum toxinMarin-Amat syndromeorbicularis resection

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Area of Science:

  • Ophthalmology
  • Neurology
  • Facial Nerve Disorders

Background:

  • Marin-Amat syndrome is a rare acquired oculofacial synkinesis.
  • It manifests as involuntary eyelid closure linked to jaw movements after peripheral facial nerve palsy.
  • Aberrant connections between cranial nerves V and VII cause increased orbicularis tone, leading to psychosocial distress.

Purpose of the Study:

  • To raise awareness about the management of Marin-Amat syndrome.
  • To highlight various treatment modalities for this rare condition.

Main Methods:

  • Presentation of six patient cases with Marin-Amat syndrome.
  • Clinical assessment including margin reflex distance (MRD) measurements.
  • Review of management options: observation, botulinum toxin injection, and surgical intervention (orbicularis resection and blepharoplasty).

Main Results:

  • Four of six patients chose observation.
  • One patient received botulinum toxin injection.
  • One patient underwent orbicularis resection and blepharoplasty, with satisfactory reduction in synkinetic movement for both treated patients.

Conclusions:

  • Marin-Amat syndrome is a rare, often underdiagnosed disorder following peripheral facial nerve palsy.
  • Botulinum toxin injection and preseptal orbicularis resection are effective management options.
  • Management strategies should be tailored to individual patient needs and preferences.