Publication
Exclusion of inv(2)(p16.1;q14.3) as the cause of a severe congenital disease by Next-Generation Sequencing
| dc.contributor.author | Pinto Cardoso, Manuela | |
| dc.contributor.author | Talkowski, Michael E. | |
| dc.contributor.author | Freixo, João | |
| dc.contributor.author | Gonçalves, Rui | |
| dc.contributor.author | Morton, Cynthia C. | |
| dc.contributor.author | David, Dezső | |
| dc.date.accessioned | 2016-02-15T12:09:25Z | |
| dc.date.available | 2016-02-15T12:09:25Z | |
| dc.date.issued | 2015-11 | |
| dc.description.abstract | <b>Introduction:</b> Congenital anomalies, a leading cause of infant mortality in developed countries, are usually caused by genomic and/or chromosome rearrangements. Such rearrangements, like inversions, disrupt the genomic architecture at the breakpoint regions and can be either subclinical or pathogenic. Currently, the lack of a fully annotated genome hinders the prediction of phenotypical consequences of these anomalies. <b>Methods:</b> We report a familial pericentric inversion, inv(2)(p16.1;q14.3), in a proband presenting multiple psychomotor and developmental anomalies, dismorphism and autistic features, with phenotypically normal parents. Traditional analysis methods are labor intensive and of low resolution. Here we employed Next-Generation Sequencing (NGS) to identify breakpoints at nucleotide resolution in the proband, followed by familial segregation analysis by Sanger sequencing. Genomic and transcriptome array analysis were performed, for exclusion of further genomic alterations and for gene expression profiling. <b>Results:</b> The inversion breakpoints, at chr2:55,707,929 and chr2:123,010,109 (GRCh38), did not disrupt any gene or regulatory element and are flanked by <i>PNPT1</i> and <i>EFEMP1</i>, and <i>TSN</i> and <i>CNTNAP5</i>, respectively. No significant alteration in the expression level of possible candidate genes were observed. Aside from a polymorphic duplication, inherited from his father, no other pathogenic genomic imbalances were identified in the proband. <b>Discussion:</b> Based on these data, the causal relationship between clinical phenotype and the inversion is most likely excluded, as the inversion probably is nonpathogenic. It was yet not possible to establish the cause of the observed phenotype. The introduction of NGS represents a hallmark in the characterization of congenital disorders associated with chromosomal rearrangements. | pt_PT |
| dc.description.sponsorship | FCT | pt_PT |
| dc.identifier.uri | http://hdl.handle.net/10400.18/3292 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.subject | Doenças Genéticas | pt_PT |
| dc.subject | Doenças Genómicas | pt_PT |
| dc.title | Exclusion of inv(2)(p16.1;q14.3) as the cause of a severe congenital disease by Next-Generation Sequencing | pt_PT |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.awardURI | info:eu-repo/grantAgreement/FCT/3599-PPCDT/HMSP-ICT%2F0016%2F2013/PT | |
| oaire.citation.conferencePlace | Porto, Portugal | pt_PT |
| oaire.citation.title | 19ª Reunião da Sociedade Portuguesa de Genética Humana, 5-7 novembro 2015 | pt_PT |
| oaire.fundingStream | 3599-PPCDT | |
| project.funder.identifier | http://doi.org/10.13039/501100001871 | |
| project.funder.name | Fundação para a Ciência e a Tecnologia | |
| rcaap.rights | openAccess | pt_PT |
| rcaap.type | conferenceObject | pt_PT |
| relation.isProjectOfPublication | 55f3392d-71be-4224-bedd-9feb4a06c428 | |
| relation.isProjectOfPublication.latestForDiscovery | 55f3392d-71be-4224-bedd-9feb4a06c428 |