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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.
Subject(s)
Full text: 1 Index: IMSEAR Main subject: Recurrence / Female / Humans / Tomography, X-Ray Computed / Child / Craniofacial Abnormalities / Dacryocystitis / Camurati-Engelmann Syndrome / Nasolacrimal Duct Language: En Journal: Indian J Ophthalmol Year: 2007 Type: Article
Full text: 1 Index: IMSEAR Main subject: Recurrence / Female / Humans / Tomography, X-Ray Computed / Child / Craniofacial Abnormalities / Dacryocystitis / Camurati-Engelmann Syndrome / Nasolacrimal Duct Language: En Journal: Indian J Ophthalmol Year: 2007 Type: Article