A new in utero sheep model for unilateral coronal craniosynostosis

Plastic and Reconstructive Surgery

Volumn 101, Issue 2, 1998, Pages 278-286

  Stelnicki, Eric J ^a   Vanderwall, Karen ^a   Hoffman, William Y ^a   Harrison, Michael R ^a   Glowacki, Julie ^a   Longaker, Michael T ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CEPHALOMETRY; CONTROLLED STUDY; CRANIOFACIAL SYNOSTOSIS; HISTOLOGY; MEASUREMENT; NONHUMAN; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SHEEP; SKULL DEVELOPMENT;

ANIMALS; CRANIAL SUTURES; CRANIOSYNOSTOSES; DISEASE MODELS, ANIMAL; FEMALE; METHODS; SHEEP; SKULL;

EID: 0031883166     PISSN: 00321052     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006534-199802000-00003     Document Type: Article

References (30)

1. Cohen, M. M., Jr. Etiopathogenesis of craniosynostosis. Neurosurg. Clin. North Am. 2: 507, 1991.
2. Cohen, M. M., Jr., and Kreiborg, S. Birth prevalence studies of the Crouzon syndrome: Comparison of direct and indirect methods. Clin. Genet. 41: 12, 1992.
3. Moss, M. L. The pathogenesis of premature cranial synostosis in man. Acta Anat. 27: 351, 1959.
4. Virchow, R. Uber den Cretinismus, namentlich in Franken, und uber pathologische Schadelformen. Verh. Phys-Med. 2: 241, 1851.
5. Mooney, M. P., Losken, H. W., Tschakaloff, A., et al. Congenital bilateral coronal suture synostosis in a rabbit and craniofacial growth comparisons with experimental models. Cleft Palate Craniofac. J. 30: 121, 1993.
6. Antikainen, T., Kallioinen, M., Waris, T., et al. A new method for the creation and measurement of experimental craniosynostosis. Childs Nerv. Syst. 8: 457, 1992.
7. Persing, J. A., Lettieri, J. T., Cronin, A. J., et al. Craniofacial suture stenosis: Morphologic effects. Plast. Reconstr. Surg. 88: 563, 1991.
8. Persing, J. A., Babler, W. J., Jane, J. A., et al. Experimental unilateral coronal synostosis in rabbits. Plast. Reconstr. Surg. 77: 369, 1986.
9. Persing, J. A., Cronin, A. J., Delashaw, J. B., et al. Late surgical treatment of unilateral coronal synostosis using methyl methacrylate. J. Neurosurg. 66: 793, 1987.
10. Choudhary, S. Apert's disease. J. Indian Med. Assoc. 88: 136, 1990.
11. Ginsberg, N. A., Zbaraz, D., and Strom, C. Transabdominal embryoscopy for the detection of Carpenter syndrome during the first trimester. J. Assist. Reprod. Genet. 11: 373, 1994.
12. Hill, L. M., Thomas, M. L., and Peterson, C. S. The ultrasonic detection of Apert syndrome. J. Ultrasound Med. 6: 601, 1987.
13. Duncan, B. W., Adzick, N. S., Moelleken, B. R., et al. An in utero model of craniosynostosis. J. Craniofac. Surg. 3: 70, 1992.
14. Brain, E. B. The Preparation of Decalcified Sections, Vol. 1, 1st. Ed. Springfield, Ill.: Charles C. Thomas, 1966. Pp. 69-141.
15. Morrow, W. W., and Broadbent, B. H., Jr. Cephalometrics. In J. Dyson (Ed.), Facial Growth, 3rd Ed. Philadelphia: Saunders, 1990. Pp. 346-395.
16. Mulliken, J. B., and Warman, M. L. Molecular genetics and craniofacial surgery. Plast. Reconstr. Surg. 97: 666, 1996.
17. Jabs, E. W., Li, X., Scott, A. F., et al. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nat. Genet. 8: 275, 1994.
18. Mooney, M. P., Losken, H. W., Siegel, M. I., et al. Development of a strain of rabbits with congenital simple nonsyndromic coronal suture synostosis: Part I. Breeding demographics, inheritance pattern, and craniofacial anomalies. Cleft Palate Craniofac J. 31: 1, 1994.
19. Roth, D. A., Han, V. K., McCarthy, J. G., McMullen, H. F., Gold, L. I., and Longaker, M. T. Studies in cranial suture biology: Part I. The immunolocalization of TGF-B1, B2, B3 in rat cranial suture development and fusion. J. Bone Miner. Res. (in press).
20. Gerhart, T. N., Kirker-Head, C. A., Kriz, M. J., et al. Healing segmental femoral defects in sheep using recombinant human bone morphogenetic protein. Clin. Orthop. 293: 317, 1993.
21. Aspenberg, P., Wang, E., and Thorngren, K. G. Bone morphogenetic protein induces bone in the squirrel monkey, but bone matrix does not. Acta Orthop. Scand. 63: 619, 1992.
22. Jabs, E.W., Muller, U., Li, X., et al. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75: 443, 1993.
23. Tureckova, J., Sahlberg, C., Aberg, T., et al. Comparison of expression of the msx-1, msx-2, BMP-2, and BMP-4 genes in the mouse upper diastemal and molar tooth primordia. Int. J. Dev. Biol. 39: 459, 1995.
24. Paley, R. J., Persing, J. A., Doctor, A., et al. Multiple sclerosis and brain tumor: A diagnostic challenge. J. Emerg. Med. 7: 241, 1989.
25. Persing, J. A., Babler, W. J., Nagorsky, M. J., et al. Skull expansion in experimental craniosynostosis. Plast. Reconstr. Surg. 78: 594, 1986.
26. Di Rocco, C., and Velardi, F. Nosographic identification and classification of plagiocephaly. Childs Nerv. Syst. 4: 9, 1988
27. Kim, H., Uppal, V., and Wallach, R. Apert syndrome and fetal hydrocephaly. Hum. Genet. 73(1): 93, 1986.
28. Stamm, E. R., Pretorius, D. H., Rumack, C. M., et al. Kleeblattschadel anomaly: In utero sonographic appearance. J. Ultrasound Med. 6: 319, 1987.
29. Sims, D. C., Butler, P. E. M., Casanova, R., Randolph, M. A., Ahn, D. K., and Yaremchuk, M. J. Surgical model to assess the effects, and optimal timing of craniofacial fixation. J. Craniofac. Surg. 7: 412, 1996.
30. Liu, Y. H., Kundu, R., Wu, L., et al. Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull. Proc. Natl. Acad. Sci. U.S.A. 92: 6137, 1995.