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The Tessier number 9 cleft.

D J David1, M H Moore, R D Cooter

  • 1South Australian Cranio-Facial Unit, Adelaide Children's Hospital.

Plastic and Reconstructive Surgery
|March 1, 1989
PubMed
Summary
This summary is machine-generated.

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This study provides the first complete description of the rare Tessier number 9 cleft, detailing its extensive soft-tissue and skeletal disruptions in craniofacial anomalies.

Area of Science:

  • Craniofacial surgery
  • Plastic surgery
  • Medical imaging

Background:

  • Tessier number 9 clefts are exceptionally rare craniofacial anomalies.
  • Previous descriptions have been incomplete, limiting understanding of their full extent.

Observation:

  • Detailed clinical, radiologic, and operative examination of two patients.
  • Mapping of soft-tissue disruption from the upper eyelid to the temporal scalp.
  • Identification of associated hairline indicators.

Findings:

  • Comprehensive description of the rarest craniofacial clefts.
  • Soft-tissue involvement includes the lateral upper eyelid, eyebrow, and temporal scalp.
  • Skeletal disruption extends from the superolateral orbital rim to the cranial base and calvaria.

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Implications:

  • Enhances understanding of rare craniofacial clefts.
  • Provides a basis for surgical planning and treatment strategies.
  • Contributes to the literature on complex craniofacial malformations.