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Tessier number 2 cleft, a variation. Case report.

P Tiwari1, S K Bhatnagar, G S Kalra

  • 1Post Graduate Dept. of Plastic Surgery, King George's Medical College, Lucknow, India.

Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|November 1, 1991
PubMed
Summary
This summary is machine-generated.

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Tessier number 2 craniofacial cleft is a rare condition affecting the nostril rim, alveolar arch, and nasal bone. This case report details a patient with bilateral clefts and mild hypertelorism.

Area of Science:

  • Craniofacial Surgery
  • Pediatric Plastic Surgery
  • Congenital Anomalies

Background:

  • Tessier number 2 craniofacial clefts are exceptionally rare congenital anomalies.
  • The etiology of these clefts remains largely unknown.
  • Distinctive soft tissue and bony features characterize this specific cleft type.

Observation:

  • The study describes a unique patient case involving a Tessier number 2 craniofacial cleft.
  • The patient presented with bilateral interruption of the middle third of the alar rim.
  • Mild asymmetrical hypertelorism was also noted in the patient.

Findings:

  • The described craniofacial cleft follows a specific anatomical path.
  • It involves the nostril rim, alveolar arch (lateral incisor level), and the junction of the nasal bone and maxillary frontal process.

Related Experiment Videos

  • The cleft extends cranially, resembling a Tessier number 12 cleft.
  • Implications:

    • Understanding the precise anatomical course is crucial for surgical planning.
    • This case highlights the importance of recognizing rare craniofacial cleft presentations.
    • Further research into the etiology of Tessier number 2 clefts is warranted.