1.
Indian J Ophthalmol
;
2007 May-Jun; 55(3): 219-21
Article
in English
| IMSEAR
| ID: sea-70351
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.
Subject(s)
Camurati-Engelmann Syndrome/complications , Child , Craniofacial Abnormalities/complications , Dacryocystitis/etiology , Female , Humans , Nasolacrimal Duct/diagnostic imaging , Recurrence , Tomography, X-Ray Computed
2.
Neurol India
;
2006 Sep; 54(3): 319-20
Article
in English
| IMSEAR
| ID: sea-120280