1.
Indian J Ophthalmol
;
2007 May-Jun; 55(3): 219-21
Article
Dans Anglais
| IMSEAR
| ID: sea-70351
Résumé
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.
Sujets)
Syndrome de Camurati-Engelmann/complications , Enfant , Malformations crâniofaciales/complications , Dacryocystite/étiologie , Femelle , Humains , Conduit nasolacrymal/imagerie diagnostique , Récidive , Tomodensitométrie
2.
Neurol India
;
2006 Sep; 54(3): 319-20
Article
Dans Anglais
| IMSEAR
| ID: sea-120280