APA 6th Edition Ivankov, A., Bobinec, A., Boban, Lj., Sansović, I. i Barišić, I. (2017). De novo složena kromosomska preraspodjela u regiji 2q32q35. Paediatria Croatica, 61 (2), 78-82. https://doi.org/10.13112/PC.2017.12
MLA 8th Edition Ivankov, Ana-Maria, et al. "De novo složena kromosomska preraspodjela u regiji 2q32q35." Paediatria Croatica, vol. 61, br. 2, 2017, str. 78-82. https://doi.org/10.13112/PC.2017.12. Citirano 08.08.2020.
Chicago 17th Edition Ivankov, Ana-Maria, Adriana Bobinec, Ljubica Boban, Ivona Sansović i Ingeborg Barišić. "De novo složena kromosomska preraspodjela u regiji 2q32q35." Paediatria Croatica 61, br. 2 (2017): 78-82. https://doi.org/10.13112/PC.2017.12
Harvard Ivankov, A., et al. (2017). 'De novo složena kromosomska preraspodjela u regiji 2q32q35', Paediatria Croatica, 61(2), str. 78-82. https://doi.org/10.13112/PC.2017.12
Vancouver Ivankov A, Bobinec A, Boban Lj, Sansović I, Barišić I. De novo složena kromosomska preraspodjela u regiji 2q32q35. Paediatria Croatica [Internet]. 2017 [pristupljeno 08.08.2020.];61(2):78-82. https://doi.org/10.13112/PC.2017.12
IEEE A. Ivankov, A. Bobinec, Lj. Boban, I. Sansović i I. Barišić, "De novo složena kromosomska preraspodjela u regiji 2q32q35", Paediatria Croatica, vol.61, br. 2, str. 78-82, 2017. [Online]. https://doi.org/10.13112/PC.2017.12
Sažetak Complex chromosomal rearrangements are rare events involving three or more cytogenetic breaks, generally on two or more chromosomes.
If breakpoints are localized and show lack of homology, they are most likely formed by the mechanism called chromothripsis.
Chromothripsis is a single catastrophic event where a part or an entire chromosome, or few chromosomes are fragmented
into multiple pieces and reassembled in a random order. Here we report on a 5.5-year-old boy with characteristic
dysmorphism, cleft palate, dental anomaly, patent ductus arteriosus, feeding diffi culties and global developmental delay. Conventional
cytogenetic analysis and chromosomal microarray analysis revealed complex chromosomal rearrangement in region
2q32q35. The boy was diagnosed with Glass syndrome, based on clinical phenotypic features and results of genetic analysis. Considering
the localization of rearrangements, the mechanism of origin could be chromothripsis. To confi rm the mechanism, additional
research with next-generation sequencing methods is required.