Fogorvosi szemle, 1994 (87. évfolyam, 1-12. szám)
1994-03-01 / 3. szám
IRODALOM: 1. Alexander, S. A., Ripa, L. W., Brenner, C.: Agenesis of a primary and permanent incisor. Oral Surg. Oral Med. Oral Pathol. 64, 377, 1987. — 2. Berry, S. A., Pierpont, M. E., Gorlin, R. JSingle central incisor in familial holoprosencephaly. J. Pediatr. 104, 877, 1984. — 3. Bőik, L.: Die überzähligen oberen Inzisivi des Menschen. Dtsch. Mschr. Zahnheilk. 35, 185, 1917. 4. Boyd, J. B., Miles, A. E. WAn Erupted Tooth in a Cyclops Foetus. Br. Dent. J. 91, 173, 1951. — 5. Bruszt, P.: Die Selbstregelung der Zahnreihe nach dem Verlust des oberen mittleren Schneidezahnes im Wechselgebiss. Schweiz. Mschr. Zahnheilk. 66, 926, 1956. — 6. Ellisdon, P. S., Marshall, К. F.: Connation of Maxillary Incisors. Br. Dent. J. 129, 16, 1970. — 7. Fleming, P., Nelson, J., Gorlin, R. J.: Single maxillary central incisor in association with mid-line anomalies. Br. Dent. J. 168, 476, 1990. — 8. Fujita, H., Ohmori, I.: Median incisor fusion. Oral Surg. Oral Med. Oral Pathol. 57, 578, 1984. — 9. Fulstow, E. D.: The Congenital Absence of an Upper Central Incisor. Br. Dent. J. 124, 186. 1968. — 10. Harndt, E., Weyers, H.: Zahn-, Mund- und Kieferheilkunde im Kindesalter. Quintessenz Verlag, Berlin, 1967. 122. — II. Kjaer, IPrenatal development of the maxillary primary incisors related to maturation of the surrounding bone and to postnatal eruption. In: The Biological Mechanisms of Tooth Eruption and Root Resorption (Ed.: Davidovitch, Z.), EBSCO Media. Birmingham. 1988, 233. - 12. Kopp, W. K.: A hereditary congenitally missing maxillary central incisor. Oral Surg. Oral Med. Oral Pathol. 24, 367, 1967. — 13. Lowry, R. B.: Holoprosencephaly. Am. J. Dis. Child. 128, 887, 1974. - 14. Maréchaux, S. C.: The single maxillary central primary incisor: report of case. J. Dent. Child. 53, 124, 1986. — 15. Mofson, E. R.. Seidberg, И.: Congenital single incisor. Oral Surg. Oral Med. Oral Pathol. 38, 490, 1974. — 16. Poyton, H. G., Morgan, G. A., Levine, N.: Median incisor fusion. Oral Surg. Oral Med. Oral Pathol. 28, 76, 1969. — 17. Radnai P. A.: Ritka fogzási rendellenességek két esete. Fogorv. Szle. 36, 62, 1943. - 18. Rappaport, E. B. et al.: Solitary maxillary central incisor and short stature. J. Pediatr. 91, 924. 1977. — 19. Santoro, F. P., Wesley, R. K.: Clinical evaluation of two patients with a single maxillary central incisor. J. Dent. Child. 50, 379, 1983. — 20. Scott, D. CAbsence of Upper Central Incisor. Br. Dent. J. 104, 247. 1958. — 21. Schulze, C.: Developmental abnormalities of the teeth and jaws. In: Thoma’s oral pathology (Ed: Gorlin, F. R., Goldman, H. M.), 6. ed. Vol. I. Mosby, St. Louis, 1970. 96 183 (117, 127). — 22. Schulze, G.: Anomalien und Missbildungen der menschlichen Zähne. Quintessenz Verlag, Berlin—Chicago—London—Sao Paulo—Tokio, 1987. 277, 377. — 23. Sedano, H. ()., Gorlin, R. JThe oral manifestations of cyclopia. Oral Surg. Oral Med. Oral Pathol. 16, 823, 1963. 24. Seger, S.: Defektbildungen an der Zahnleiste und an den Extremitäten. Med. Diss. Berlin, 1955. Cit.: Schulze, C., 1987. — 25. Small, B. WCongenitally missing maxillary central incisor. Oral Surg. Oral Med. Oral Pathol. 48, 97. 1979. 26. Stahl, A.: Dysplasien im Bereich des Mundes, der Kiefer und der Zähne bei Dysmelie. (Ein Beitrag zur Thalidomid-Embryopathie). Dtsch. zahnärztl. Z. 22, 356, 1967. — 27. Törő I Az ember fejlődése. Medicina, Budapest, 1964. 135. — 28. Vanelli, M., Bernasconi, S., Balestrazzi, P.: Incisive supérieure unique et déficit en STH. Arch. Fr. Pediatr. 37, 321, 1980. — 29. Veno, H., Mochizuki, I., Morimoto, MDental anomalies in the midline. Oral Surg. Oral Med. Oral Pathol. 65, 638. 1988. — 30. Wesley, R. K. et al.: Solitary maxillary central incisor and normal stature. Oral Surg. Oral Med. Oral Pathol. 46, 837, 1978. — 31. Winter, W. E. et al.: Solitary central maxillary incisor associated with precocious puberty and hypothalamic hamartoma. J. Pediatr. 101, 965, 1982. Dr. Kocsis. 8. G.: Single central maxillary incisor in the midline as the mild form of the holoprosencephaly Besides the hypotelorism the mildest form of holoprosencephaly is the solitary incisor. In the case described, the girl had only high palate and torus palatinus, hut no other alteration in the midline. One of her brothers had cleft lip and palate, which indicates genetical determination. The girl has been orthodontically treated. 70
