Predominant or exclusive orrbital and facial involvement in infantile cortical hyperostosis (de Toni-Caffey's disease) Report of four cases and a review of the literature

Author:

Faur� C.,Beyssac J. M.,Montagne J. P.

Publisher

Springer Science and Business Media LLC

Subject

Radiology Nuclear Medicine and imaging,Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Berio, A., Pelizza, A., Di Stefano, A.: La sindrome di de Toni-Caffey-Silverman. Osservazione di uncaso coon isolato interessamento della mandibol. Minerva Pediatr.23, 1567 (1971)

2. Boyd, R. D. H., Shaw, D. G., Thomas, B. M.: Infantile cortical hyperostosis with lytic lesions in to sskull. Arch. Dis. Child.47, 471 (1972)

3. Boyes, J. G., Demy, N. G.: Infantile cortical hyperostosis: A familial disease? Am. J. Roentgenol. Radium Ther. Nucl. Med.65, 924 (1951)

4. Brooksaler, F., Miller, J. E.: Infantile corticalhypeerostosis. J. Pediatr.48, 739 (1956)

5. Caffey, J.: Pediatric X-ray diagnosis, 6gh ed. Chicago: Year Book Medical Publisher 1972

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