Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-29T01:48:23.108Z Has data issue: false hasContentIssue false

Long-Term Survival and Late Onset Seizures in an Adolescent with Trisomy 13

Published online by Cambridge University Press:  02 December 2014

Francois Dominique Jacob
Affiliation:
Division of Pediatric Neurology, University of Alberta, Edmonton, Alberta, Canada
Vijay Ramaswamy
Affiliation:
Division of Pediatric Neurology, University of Alberta, Edmonton, Alberta, Canada
Hanna Kolski*
Affiliation:
Division of Pediatric Neurology, University of Alberta, Edmonton, Alberta, Canada
*
Division of Pediatric Neurology, Department of Pediatrics, Stollery Children’s Hospital, #8213 Aberhart Centre 1, 11402 University Ave NW, Edmonton, Alberta, T6G 2J3, Canada.
Rights & Permissions [Opens in a new window]

Abstract

Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Brief Communications
Copyright
Copyright © The Canadian Journal of Neurological 2010

References

1. Patau, K, Smith, DW, Therman, E, Inhorn, SL, Wagner, HP. Multiple congenital anomaly caused by an extra autosome. Lancet. 1960 Apr 9;1:7903.Google Scholar
2. Jones, KL, Smith, DW. Smith’s recognizable patterns of human malformation. 6th ed. Philadelphia: Elsevier Saunders; 2006. p.1821.Google Scholar
3. Jacobs, PA, Hassold, TJ, Henry, A, Pettay, D, Takaesu, N. Trisomy 13 ascertained in a survey of spontaneous abortions. J Med Genet. 1987 Dec;24(12):7214.Google Scholar
4. Brewer, CM, Holloway, SH, Stone, DH, Carothers, AD, FitzPatrick, DR. Survival in trisomy 13 and trisomy 18 cases ascertained from population based registers. J Med Genet. 2002 Sep;39(9):e54.CrossRefGoogle ScholarPubMed
5. Baty, BJ, Blackburn, BL, Carey, JC. Natural history of trisomy 18 and trisomy 13: I. Growth, physical assessment, medical histories, survival, and recurrence risk. Am J Med Genet. 1994 Jan 15;49 (2):17588.Google Scholar
6. Baty, BJ, Jorde, LB, Blackburn, BL, Carey, JC. Natural history of trisomy 18 and trisomy 13: II. Psychomotor development. Am J Med Genet. 1994 Jan 15;49(2):18994.CrossRefGoogle ScholarPubMed
7. Iliopoulos, D, Sekerli, E, Vassiliou, G, et al. Patau syndrome with a long survival (146 months): a clinical report and review of literature. Am J Med Genet. 2006 Jan 1;140(1):923.Google Scholar
8. Marden, PM, Yunis, JJ. Trisomy D1 in a 10-year-old girl. Normal neutrophils and fetal hemoglobin. Am J Dis Child. 1967 Dec;114 (6):6624.Google Scholar
9. Redheendran, R, Neu, RL, Bannerman, RM. Long survival in trisomy-13-syndrome: 21 cases including prolonged survival in two patients 11 and 19 years old. Am J Med Genet. 1981;8(2):16772.Google Scholar
10. Singh, KS. Trisomy 13 (Patau’s syndrome): a rare case of survival into adulthood. J Ment Defic Res. 1990 Feb;34(Pt 1):913.Google Scholar
11. Tunca, Y, Kadandale, JS, Pivnick, EK. Long-term survival in Patau syndrome. Clin Dysmorphol. 2001 Apr;10(2):14950.Google Scholar
12. Zoll, B, Wolf, J, Lensing-Hebben, D, Pruggmayer, M, Thorpe, B. Trisomy 13 (Patau syndrome) with an 11-year survival. Clin Genet. 1993 Jan;43(1):4650.Google Scholar
13. Lindor, N, Karnes, P, Jalal, S, Dewald, G, Shaughnessy, W, Michels, V. Trisomy 13 in a 16-year-old boy. Dysmorphol Clin Genet. 1992 1992;6(4):4.Google Scholar
14. Fogu, G, Maserati, E, Cambosu, F, et al. Patau syndrome with long survival in a case of unusual mosaic trisomy 13. Eur J Med Genet. 2008 Jul-Aug;51(4):30314.CrossRefGoogle Scholar
15. Delatycki, M, Gardner, RJ. Three cases of trisomy 13 mosaicism and a review of the literature. Clin Genet. 1997 Jun;51(6):4037.Google Scholar
16. Hook, EB. Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use. Am J Med Genet. 1977 Jan;29(1):947.Google ScholarPubMed
17. Croen, LA, Shaw, GM, Lammer, EJ. Holoprosencephaly: epidemiologic and clinical characteristics of a California population. Am J Med Genet. 1996 Aug 23;64(3):46572.Google Scholar
18. Inagaki, M, Ando, Y, Mito, T, et al. Comparison of brain imaging and neuropathology in cases of trisomy 18 and 13. Neuroradiology. 1987;29(5):4749.Google Scholar
19. Hori, A, Peiffer, J, Pfeiffer, RA, Iizuka, R. Cerebello-cortical heterotopia in dentate nucleus, and other microdysgeneses in trisomy D1 (Patau) syndrome. Brain Dev. 1980;2(4):34552.CrossRefGoogle ScholarPubMed
20. Sener, RN. Bilateral, perisylvian and rolandic cortical dysplasia in trisomy 13 syndrome. J Neuroradiol. 1996 Dec;23(4):2313.Google Scholar