EED and EZH2 constitutive variants: A study to expand the Cohen-Gibson syndrome phenotype and contrast it with Weaver syndrome
- PMID: 30793471
- DOI: 10.1002/ajmg.a.61066
EED and EZH2 constitutive variants: A study to expand the Cohen-Gibson syndrome phenotype and contrast it with Weaver syndrome
Abstract
Overgrowth-intellectual disability (OGID) syndromes are characterized by increased growth (height and/or head circumference ≥+2 SD) in association with an intellectual disability. Constitutive EED variants have previously been reported in five individuals with an OGID syndrome, eponymously designated Cohen-Gibson syndrome and resembling Weaver syndrome. Here, we report three additional individuals with constitutive EED variants, identified through exome sequencing of an OGID patient series. We compare the EED phenotype with that of Weaver syndrome (56 individuals), caused by constitutive EZH2 variants. We conclude that while there is considerable overlap between the EED and EZH2 phenotypes with both characteristically associated with increased growth and an intellectual disability, individuals with EED variants more frequently have cardiac problems and cervical spine abnormalities, boys have cryptorchidism and the facial gestalts can usually be distinguished.
Keywords: EED; EZH2; Cohen-Gibson; Weaver; intellectual disability; overgrowth.
© 2019 Wiley Periodicals, Inc.
Similar articles
-
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.Am J Med Genet A. 2013 Dec;161A(12):2972-80. doi: 10.1002/ajmg.a.36229. Epub 2013 Nov 8. Am J Med Genet A. 2013. PMID: 24214728
-
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes.Am J Hum Genet. 2020 May 7;106(5):596-610. doi: 10.1016/j.ajhg.2020.03.008. Epub 2020 Apr 2. Am J Hum Genet. 2020. PMID: 32243864 Free PMC article.
-
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.Hum Mutat. 2017 Jun;38(6):637-648. doi: 10.1002/humu.23200. Epub 2017 Mar 15. Hum Mutat. 2017. PMID: 28229514
-
PRC2-complex related dysfunction in overgrowth syndromes: A review of EZH2, EED, and SUZ12 and their syndromic phenotypes.Am J Med Genet C Semin Med Genet. 2019 Dec;181(4):519-531. doi: 10.1002/ajmg.c.31754. Epub 2019 Nov 14. Am J Med Genet C Semin Med Genet. 2019. PMID: 31724824 Review.
-
Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome.J Hum Genet. 2018 Apr;63(4):517-520. doi: 10.1038/s10038-017-0391-x. Epub 2018 Feb 6. J Hum Genet. 2018. PMID: 29410511 Review.
Cited by
-
A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition.JCI Insight. 2024 Jan 9;9(1):e173392. doi: 10.1172/jci.insight.173392. JCI Insight. 2024. PMID: 38015625 Free PMC article.
-
Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and review.BMC Med Genomics. 2024 Mar 6;17(1):73. doi: 10.1186/s12920-024-01843-5. BMC Med Genomics. 2024. PMID: 38448973 Free PMC article.
-
Identification of genes and pathways involved in malignant pleural mesothelioma using bioinformatics methods.BMC Med Genomics. 2021 Apr 13;14(1):104. doi: 10.1186/s12920-021-00954-7. BMC Med Genomics. 2021. PMID: 33849532 Free PMC article.
-
Loss of Polycomb Repressive Complex 2 Function Alters Digestive Organ Homeostasis and Neuronal Differentiation in Zebrafish.Cells. 2021 Nov 12;10(11):3142. doi: 10.3390/cells10113142. Cells. 2021. PMID: 34831364 Free PMC article.
-
Computational prognostic evaluation of Alzheimer's drugs from FDA-approved database through structural conformational dynamics and drug repositioning approaches.Sci Rep. 2023 Oct 21;13(1):18022. doi: 10.1038/s41598-023-45347-1. Sci Rep. 2023. PMID: 37865690 Free PMC article.
Publication types
MeSH terms
Substances
Supplementary concepts
Grants and funding
LinkOut - more resources
Full Text Sources
Medical