Case Report
A Unique Case of Unilateral Treacher-Collins Syndrome with Middle Ear Aplasia: A Case Report
Anagha J, Chinmayee C*, Nikhil M, and Mahak B
Department of Radiology, LTMMC and LTMGH, Sion, Mumbai, India
*Corresponding author:Chinmayee Chitnis, Fellow, Department of Radiology, LTMMC and LTMGH, Sion, Mumbai, India, E-mail: chinmayeechitnis5694@gmail.com
Copyright: ©2024 Anagha J, et al. This is an open-access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Article Information:Submission: 11/12/2023; Accepted: 17/01/2024; Published: 22/01/2024
Abstract
Treacher-Collins syndrome or Mandibulofacial dysostosis (MFD) is a rare congenital disorder with autosomal dominant inheritance, associated with aberrations of craniofacial development. The most common clinical features include malar bone and mandibular hypoplasia, antimongoloid slanting of palpebral fissures, and other ear abnormalities. Computed tomography is the imaging modality of choice for the morphological analysis of the craniofacial bones in individuals with complex facial deformities and to assist in the planning of surgical intervention. We present a case of unilateral mandibulofacial dysostosis with absent middle ear ossicles.
Keywords:Treacher-Collins; Middle Ear Ossicles; Computed Tomography; Zygomatic bone
