Abstract
Treacher Collins syndrome is a rare autosomal dominant disorder of craniofacial development. The fully expressed phenotype exhibits characteristic dysmorphic features involving the face, eyes, mandible and ears. We report a case of a 17-year-old woman presenting with the typical orofacial implications of this syndrome. Copyright 2013 BMJ Publishing Group. All rights reserved.
Cite
CITATION STYLE
APA
Mohan, R. P. S., Verma, S., Agarwal, N., & Singh, U. (2013). Treacher Collins syndrome: A case report. BMJ Case Reports. https://doi.org/10.1136/bcr-2013-009341
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free