[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 23.23.54.109. Please contact the publisher to request reinstatement.
Sign In
Individual Sign In
Create an Account
Institutional Sign In
OpenAthens Shibboleth
[Skip to Content Landing]
Special Feature
August 1999

Picture of the Month

Author Affiliations

From the Departments of Pediatric Surgery (Drs Méndez, Aymerich, and Garrido) and Pediatrics (Dr Bello), Hospital Materno-Infantil "Teresa Herrera" Complejo Hospitalario "Juan Canalejo," La Coruña, Spain; and the American Board of Pediatrics, Chapel Hill, NC (Dr Tunnessen).

 

WALTER W.TUNNESSENMD

Arch Pediatr Adolesc Med. 1999;153(8):889-890. doi:10.1001/archpedi.153.8.889

AN 8-YEAR-OLD GIRL was referred for evaluation of congenital facial deformities. She was born after an uneventful pregnancy during which her mother received no medications and was not exposed to radiation. There was no family history of congenital anomalies.

On physical examination the girl had unilateral macrostomia as a result of a transverse right stomal cleft and a severe deformity of the right auricle, including supernumerary auricular cartilage anterior to the tragus and absence of the right ear canal (Figure 1 and Figure 2). The left ear was normal. There was no evidence of midfacial skeletal hypoplasia. The ascending ramus of the mandible and the temporomandibular joint were normal. The palate was intact. Conductive hearing loss was present in the right ear. The remainder of the physical examination results were unremarkable.

×