| Literature DB >> 17456942 |
Abstract
We describe a rare syndrome characterized by severe craniofacial hyperostosis, sclerosis, obliteration of paranasal sinuses and foramina of skull base, in a 10-year-old female child who presented with abnormal facial features and recurrent dacryocystitis due to narrowing of nasolacrimal duct.Entities:
Mesh:
Year: 2007 PMID: 17456942 DOI: 10.4103/0301-4738.31945
Source DB: PubMed Journal: Indian J Ophthalmol ISSN: 0301-4738 Impact factor: 1.848