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Published on: October 18, 2021
Le Fort II Distraction with Simultaneous Zygomatic Repositioning
Richard A Hopper1, Howard D Wang1, Ezgi Mercan2
1The Craniofacial Center, Seattle Children's Hospital, 4800 Sand Point Way Northeast, Seattle, WA 98105, USA; Division of Plastic Surgery, Department of Surgery, University of Washington, Seattle, WA, USA.
Le Fort II distraction with zygomatic repositioning corrects midface hypoplasia by allowing independent movement of central and lateral facial segments. This modified Le Fort III procedure is ideal for Apert facial dysmorphology.
Area of Science:
- Craniofacial Surgery
- Orthognathic Surgery
- Pediatric Plastic Surgery
Background:
- Severe midface hypoplasia presents challenges in correcting abnormal facial proportions.
- Le Fort III distraction is a common surgical approach for midface hypoplasia.
- Apert facial dysmorphology often involves complex midface deficiencies.
Purpose of the Study:
- To present a modified Le Fort III distraction technique, termed Le Fort II distraction with zygomatic repositioning.
- To address specific patterns of midface deficiency where central hypoplasia is greater than lateral hypoplasia.
- To establish this modified procedure as a preferred surgical option for Apert facial dysmorphology.
Main Methods:
- The procedure involves initial Le Fort III osteotomies.
- Bilateral zygomas are subsequently separated and fixated.
- A central nasomaxillary Le Fort II segment is distracted for independent midface segment movement.
Main Results:
- This technique allows for differential distraction of central and lateral midface segments.
- It effectively corrects disproportionate midface deficiencies.
- The procedure has been adopted as the preferred method for Apert facial dysmorphology.
Conclusions:
- Le Fort II distraction with zygomatic repositioning offers a refined approach to managing severe midface hypoplasia.
- This modification provides enhanced control over central and lateral midface advancement.
- It is a highly effective treatment for patients with Apert facial dysmorphology and similar complex craniofacial conditions.
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