Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/40814

TitleRedefining the MED13L syndrome
Author(s)Lopes, Fátima Daniela Teixeira
Adegbola, Abidemi
Musante, Luciana
Maciel, P.
Hao Hu
Isidor, Bertrand
Picker-Minh, Sylvie
Caignec, Cedric Le
Lopes, Fátima
Chiaie, Barbara Delle
Issue date2015
PublisherPalgrave Macmillan
JournalEuropean Journal of Human Genetics
Abstract(s)Congenital cardiac and neurodevelopmental deficits have been recently linked to the mediator complex subunit 13-like protein MED13L, a subunit of the CDK8-associated mediator complex that functions in transcriptional regulation through DNA-binding transcription factors and RNA polymerase II. Heterozygous MED13L variants cause transposition of the great arteries and intellectual disability (ID). Here, we report eight patients with predominantly novel MED13L variants who lack such complex congenital heart malformations. Rather, they depict a syndromic form of ID characterized by facial dysmorphism, ID, speech impairment, motor developmental delay with muscular hypotonia and behavioral difficulties. We thereby define a novel syndrome and significantly broaden the clinical spectrum associated with MED13L variants. A prominent feature of the MED13L neurocognitive presentation is profound language impairment, often in combination with articulatory deficits.
TypeArticle
URIhttp://hdl.handle.net/1822/40814
DOI10.1038/ejhg.2015.26
ISSN1476-5438
Publisher versionhttp://www.nature.com/ejhg/index.html
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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