| Literature DB >> 28478456 |
Viola Alesi1, Valeria Orlando, Silvia Genovese, Sara Loddo, Elisa Pisaneschi, Daniele Pompili, Cecilia Surace, Fabrizia Restaldi, Maria C Digilio, Bruno Dallapiccola, Maria L Dentici, Antonio Novelli.
Abstract
Complex chromosomal rearrangements (CCRs) are structural aberrations involving more than 2 chromosomal breakpoints. They are associated with different outcomes depending on the deletion/duplication of genomic material, gene disruption, or position effects. Balanced CCRs can also undergo missegregation during meiotic division, leading to unbalanced derivative chromosomes and, in some cases, to affected offspring. We report on a patient presenting with developmental and speech delay, growth retardation, microcephaly, hypospadias, and dysmorphic features, harboring an interstitial 10q21.1q23.31 duplication, due to recombination of a paternal CCR. Application of several cytogenetic and molecular techniques allowed determining the biological bases of the rearrangement, understanding the underlying chromosomal mechanism, and assessing the reproductive risk.Entities:
Keywords: Chromosome 10q; Complex chromosome rearrangement; Interstitial duplication; Meiotic recombination
Mesh:
Year: 2017 PMID: 28478456 DOI: 10.1159/000475490
Source DB: PubMed Journal: Cytogenet Genome Res ISSN: 1424-8581 Impact factor: 1.636