Research Article

De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report

Volume: 7 Number: 1,EK June 1, 2013
  • Ali Karaman
  • Tülay Tos
EN TR

De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report

Abstract

Complex chromosome rearrangements (CCRs) involve more than two breakpoints on two or more chromosomes are uncommon occurrences. We report a female with developmental delay with a complex three-way balanced translocation [46,XX,t(1;4;20)(p32;q32;q12)] identified by karyotyping.This paper is the first report of reciprocal translocation involving 1p, 4q and 20q associated with the developmental delay. The developmental delay may be due to the rearrangement of genetic material at these breakpoints and this incident may cause developmental delay

Keywords

References

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Details

Primary Language

English

Subjects

Clinical Sciences

Journal Section

Research Article

Authors

Ali Karaman This is me

Tülay Tos This is me

Publication Date

June 1, 2013

Submission Date

June 1, 2013

Acceptance Date

-

Published in Issue

Year 2013 Volume: 7 Number: 1,EK

APA
Karaman, A., & Tos, T. (2013). De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report. Türkiye Çocuk Hastalıkları Dergisi, 7(1,EK), 7-10. https://izlik.org/JA29JN89PZ
AMA
1.Karaman A, Tos T. De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report. Turkish J Pediatr Dis. 2013;7(1,EK):7-10. https://izlik.org/JA29JN89PZ
Chicago
Karaman, Ali, and Tülay Tos. 2013. “De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;Q32)] in a Patient With Developmental Delay: A Case Report”. Türkiye Çocuk Hastalıkları Dergisi 7 (1,EK): 7-10. https://izlik.org/JA29JN89PZ.
EndNote
Karaman A, Tos T (June 1, 2013) De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report. Türkiye Çocuk Hastalıkları Dergisi 7 1,EK 7–10.
IEEE
[1]A. Karaman and T. Tos, “De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report”, Turkish J Pediatr Dis, vol. 7, no. 1,EK, pp. 7–10, June 2013, [Online]. Available: https://izlik.org/JA29JN89PZ
ISNAD
Karaman, Ali - Tos, Tülay. “De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;Q32)] in a Patient With Developmental Delay: A Case Report”. Türkiye Çocuk Hastalıkları Dergisi 7/1,EK (June 1, 2013): 7-10. https://izlik.org/JA29JN89PZ.
JAMA
1.Karaman A, Tos T. De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report. Turkish J Pediatr Dis. 2013;7:7–10.
MLA
Karaman, Ali, and Tülay Tos. “De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;Q32)] in a Patient With Developmental Delay: A Case Report”. Türkiye Çocuk Hastalıkları Dergisi, vol. 7, no. 1,EK, June 2013, pp. 7-10, https://izlik.org/JA29JN89PZ.
Vancouver
1.Ali Karaman, Tülay Tos. De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report. Turkish J Pediatr Dis [Internet]. 2013 Jun. 1;7(1,EK):7-10. Available from: https://izlik.org/JA29JN89PZ


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