| Literature DB >> 23709540 |
Ravi Prakash Sasankoti Mohan1, Sankalp Verma, Neha Agarwal, Udita Singh.
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.Entities:
Mesh:
Year: 2013 PMID: 23709540 PMCID: PMC3669902 DOI: 10.1136/bcr-2013-009341
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X