| Literature DB >> 29410511 |
Anna Biernacka1,2, Mateusz Biela3, Robert Smigiel4, Victor Murcia-Pienkowski1,2, Elzbieta Szmida5, Piotr Gasperowicz1, Joanna Kosinska1, Grazyna Kostrzewa6, Agnieszka Anna Koppolu1,2, Anna Walczak1, Dominik Wawrzuta1, Malgorzata Rydzanicz1, Malgorzata Sasiadek5, Rafal Ploski7.
Abstract
Overgrowth, macrocephaly, accelerated osseous maturation, variable intellectual disability, and characteristic facial features are the main symptoms of Weaver syndrome, a rare condition caused by mutations in EZH2 gene. Recently, in four patients with Weaver-like symptoms without mutations in EZH2 gene, pathogenic variants in EED were described. We present another patient clinically diagnosed with Weaver syndrome in whom WES revealed an EED de novo mutation affecting two neighboring aminoacids, NM_003797.3:c.917_919delinsCGG/p.(Arg306_Asn307delinsThrAsp) located in one allele (in cis). Our observation, together with previous reports suggests that EED gene testing is warranted in patients with the overgrowth syndrome features and suspicion of Weaver syndrome with normal results of EZH2 gene sequencing.Entities:
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Year: 2018 PMID: 29410511 DOI: 10.1038/s10038-017-0391-x
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172