Fogorvosi szemle, 1996 (89. évfolyam, 1-12. szám)

1996-03-01 / 3. szám

S., Rowalde, E.\ Familial hypophosphatemic vitamin D-resistant rickets: review of the literature and report of case. J. Dent. Child. 57, 212, 1990. - 9. Fayle, S. A., Pollard, M. A.: Congenital erythropoetic porphyia-oral manifestations and dental treatment in child-hood: A case report. Quintessence Int. 25, 551, 1994. - 10. Fleming, P., Witkap, C. J., Kuhlmann Jr., W. H.: Staining and hypoplasia of enamel caused by tetracycline a case report. Pediatr. Dent. 9, 245, 1987. - 11. Levis, L. S., Yargenson, R. J., Salinas, C. J.: Oral findings in the Morquio syndrome (mucopoly­saccharidosis IV). Oral Surg. Oral Med. Oral Pathol. 39, 390, 1975. - 12. Opinya, G. N., Valderhaug, J., Birkeland, J. M., Lakken, P. \ Fluorosis of deciduous teeth and first permanent molars in a rural Kenyan community. Acta Odontol. Scand. 49, 197, 1991. - 13. Seow, K. W.: Clinical diagnosis and management strategies of ameloge­nesis imperfecta variants. Pediatr. Dent. 15, 384, 1993. — 14. Seow, K. W.'. Dental development in amelogenesis imperfecta: a controlled study. Pediatr. Dent. 17, 26, 1995. - 15. Skinner, M. F., Fladaway, W., Dickie, J.: Effects of ethnicity and birth month on localized enamel hypoplasia of the primary canine. J. Dent. Child. 61, 109, 1994. - 16. Walls, A. W., Soames, J. W.: Dental manifestation of autoimmune hypo­­parathyroidsm. Oral Surg. Oral Med. Oral Pathol. 75, 779, 1993. - 17. Wright, J. T., Johnson, L. B., Fine, J. D. : Development defects of enamel in humans with heredi­tary epidermolysis bullosa. Arch. Oral Biol. 38, 945, 1993. — 18. Harrison’sPrincip­les of inetrnal medicine. Me. Graw-Hill Book Company, p. 1877. Dr. Albert, M., dr. Dicsőffy, Zs., dr. Keszthelyi, G.: About enamel hypoplasia in connection with one case. The developmental anomalies of dental hard tissues are reletively common in children. These anomalies can involve separately the enamel and they are due to many factors acting during odontogenesis. The paper deals with the main ethnological factors and describes a case of idiopathic hypercalcemia. It is normally accompanied by aortic stenosis, mental retardation and a characteristic elfin face. This is called Williams syndrome. In this case we only found enamel hypoplasia on the cusps of the first molars. 88

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