Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/57873

TitleThe contribution of 7q33 copy number variations for intellectual disability
Author(s)Lopes, Fátima Daniela Teixeira
Torres, Fátima
Lynch, Sally Ann
Jorge, Arminda
Sousa, Susana
Silva, João
Rendeiro, Paula
Tavares, Purificação
Fortuna, Ana Maria
Maciel, P.
Keywords7q33 CNVs
CALD1
AGBL3
EXOC4
CNOT4
Duplication
Issue dateJan-2018
PublisherSpringer Heidelberg
JournalNeurogenetics
CitationLopes, F., Torres, F., Lynch, S. A., Jorge, A., et. al.(2018). The contribution of 7q33 copy number variations for intellectual disability. neurogenetics, 19(1), 27-40
Abstract(s)Copy number variations (CNVs) at the 7q33 cytoband are very rarely described in the literature, and almost all of the cases comprise large deletions affecting more than just the q33 segment. We report seven patients (two families with two siblings and their affected mother and one unrelated patient) with neurodevelopmental delay associated with CNVs in 7q33 alone. All the patients presented mild to moderate intellectual disability (ID), dysmorphic features, and a behavioral phenotype characterized by aggressiveness and disinhibition. One family presents a small duplication in cis affecting CALD1 and AGBL3 genes, while the other four patients carry two larger deletions encompassing EXOC4, CALD1, AGBL3, and CNOT4. This work helps to refine the phenotype and narrow the minimal critical region involved in 7q33 CNVs. Comparison with similar cases and functional studies should help us clarify the relevance of the deleted genes for ID and behavioral alterations.
TypeArticle
URIhttp://hdl.handle.net/1822/57873
DOI10.1007/s10048-017-0533-5
ISSN1364-6745
e-ISSN1364-6753
Publisher versionhttps://link.springer.com/article/10.1007/s10048-017-0533-5
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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