Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 1993 Jul;30(4):414-5.
doi: 10.1597/1545-1569_1993_030_0414_ofcaro_2.3.co_2.

Oblique facial clefts: a report of Tessier numbers 3, 4, 5, and 9 clefts

Affiliations
Case Reports

Oblique facial clefts: a report of Tessier numbers 3, 4, 5, and 9 clefts

M A Darzi et al. Cleft Palate Craniofac J. 1993 Jul.

Abstract

The oblique facial cleft is an extremely rare and disfiguring congenital anomaly of the face. Tessier (1990) proposed an anatomic classification of the facial, craniofacial, and laterofacial clefts that was a great advance in the study of these clefts. The clefts were found to occur with an incidence of 1.43 to 4.85 in 100,000 births (Kawamoto, 1976). The exact incidence of these unusual facial clefts is unknown, and estimates vary widely because of the rarity of their occurrence and the lack of standard methods of data collection. To adequately examine the occurrence of oblique clefts, the medical community must be aware of the problem, and new cases should be presented. On the basis of clinical, radiologic, and surgical examinations, soft tissue and skeletal disruptions of three patients with the most rare craniofacial clefts (Tessier 3, 4, 5, and 9) are presented.

PubMed Disclaimer

Similar articles

Cited by

Publication types

LinkOut - more resources