Nasolacrimal obstruction and facial bone histopathology in craniodiaphyseal dysplasia.

Author:

McHugh D A,Rose G E,Garner A

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference10 articles.

1. Craniodiaphyseal dysplasia, a disease or a group of diseases?;Macpherson, R.I.;J Canad Assoc Radiol,1974

2. Craniodiaphyseal dysplasia;Brueton, L.A.; Winter, R.M.;J Med Genet,1990

3. Ophthalmological complications in the sclerosing bone dysplasia;Beighton, P.; Hamersma, H.;Ophthalmol Paedr Gen,1985

4. Dacryocystorhinostomy in osteopetrosis;Orengo, S.D.; Patrinely, JR;Ophthalmic Surg,1991

5. Leontiosis ossea case reports;de Souza 0;PortoAllegre (Brazil) Fac Med,1972

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1. Craniodiaphyseal dysplasia, a very rare form of bone dysplasia;Oral and Maxillofacial Surgery Cases;2020-03

2. Syndromic and Nonsyndromic Systemic Associations of Congenital Lacrimal Drainage Anomalies: A Major Review;Ophthalmic Plastic & Reconstructive Surgery;2017-11

3. Treatment of Craniodiaphyseal Dysplasia Presenting with Chiari Type-I;Arquivos Brasileiros de Neurocirurgia: Brazilian Neurosurgery;2016-07-26

4. Buried Probe in Complex Congenital Nasolacrimal Duct Obstructions;Ophthalmic Plastic & Reconstructive Surgery;2015-07

5. Simple vs complex congenital nasolacrimal duct obstructions: etiology, management and outcomes;International Forum of Allergy & Rhinology;2014-11-03

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