Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.18/1639
Título: CNV Characterization, Inheritance and Phenotypic Correlations in Families With Autism
Autor: C. Conceição, Inês
Correia, Catarina
Oliveira, Bárbara
M. Rama, Maria
Café, Cátia
Almeida, Joana
Mouga, Susana
Duque, Frederico
Oliveira, Guiomar
M. Vicente, Astrid
Palavras-chave: Perturbações do Desenvolvimento Infantil e Saúde Mental
Autism
Autism Spectrum Disorders
ASD
Data: Jun-2013
Editora: Instituto Nacional de Saúde Doutor Ricardo Jorge, IP
Resumo: Autism Spectrum Disorders (ASD) have a strong genetic component, with an estimated heritability of over 90%1. Recent studies carried out by the Autism Genome Project (AGP) consortium suggest that rare Copy Number Variants (CNVs), characterized by submicroscopic chromosomal deletions and duplications, are more frequent in ASD compared to controls, and may play an important role in susceptibility to this disorder2. However, to adequately assess pathogenicity, a detailed characterization of patients CNVs and phenotype is required. The goal of this study was to establish the clinical and etiological relevance for ASD of potentially pathogenic CNVs identified in a Portuguese population sample by whole genome CNV analysis, through the detailed characterization of CNVs and correlation with clinical phenotypes. Analysis of the AGP genome-wide CNV results using 1M SNP microarray2 identified a total of 14218 CNVs in 342 Portuguese probands. We selected 291 CNVs, present in 191 individuals (19 females and 172 males), using the following criteria: 1) CNVs that contained implicated/candidate genes for ASD; 2) CNVs in genomic regions known to be implicated/candidate for ASD; 3) CNVs in regions associated with syndromes with ASD symptoms; and 4) high confidence CNVs that did not overlap more than 20% with controls in available databases. We explored recurrence rates, genic content, regulatory elements, inheritance patterns and phenotypic correlations.
URI: http://hdl.handle.net/10400.18/1639
Aparece nas colecções:DPSPDNT - Posters/abstracts em congressos internacionais

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