Craniodiaphyseal dysplasia: an unusual cause of recurrent dacryocystitis.
Indian J Ophthalmol
; 2007 May-Jun; 55(3): 219-21
Article
in En
| IMSEAR
| ID: sea-70351
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:
1
Index:
IMSEAR
Main subject:
Recurrence
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Female
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Humans
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Tomography, X-Ray Computed
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Child
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Craniofacial Abnormalities
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Dacryocystitis
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Camurati-Engelmann Syndrome
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Nasolacrimal Duct
Language:
En
Journal:
Indian J Ophthalmol
Year:
2007
Type:
Article