Craniodiaphyseal dysplasia: an unusual cause of recurrent dacryocystitis.
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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Recurrence
/
Female
/
Humans
/
Tomography, X-Ray Computed
/
Child
/
Craniofacial Abnormalities
/
Dacryocystitis
/
Camurati-Engelmann Syndrome
/
Nasolacrimal Duct
Language:
English
Journal:
Indian J Ophthalmol
Year:
2007
Type:
Article
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