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EED and EZH2 constitutive variants: A study to expand the Cohen-Gibson syndrome phenotype and contrast it with Weaver syndrome.
Griffiths, Sara; Loveday, Chey; Zachariou, Anna; Behan, Lucy-Ann; Chandler, Kate; Cole, Trevor; D'Arrigo, Stefano; Dieckmann, Andrea; Foster, Alison; Gibney, James; Hunter, Matthew; Milani, Donatella; Pantaleoni, Chiara; Roche, Edna; Sherlock, Mark; Springer, Amanda; White, Susan M; Tatton-Brown, Katrina.
Afiliação
  • Griffiths S; Department of Clinical Genetics, St George's University of London, London, United Kingdom.
  • Loveday C; Division of Genetics and Epidemiology, Institute of Cancer Research, Sutton, United Kingdom.
  • Zachariou A; Division of Clinical Studies, Institute of Cancer Research, Sutton, United Kingdom.
  • Behan LA; Department of Endocrinology, Beaumont Hospital, Dublin, Ireland.
  • Chandler K; Department of Paediatric Growth, Diabetes and Endocrinology, Tallaght University Hospital, Dublin, Ireland.
  • Cole T; Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom.
  • D'Arrigo S; Department of Clinical Genetics, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, United Kingdom.
  • Dieckmann A; Developmental Neurology Unit, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
  • Foster A; Department of Neuropediatrics, Jena University Hospital, Jena, Germany.
  • Gibney J; Department of Clinical Genetics, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, United Kingdom.
  • Hunter M; Department of Paediatric Growth, Diabetes and Endocrinology, Tallaght University Hospital, Dublin, Ireland.
  • Milani D; Department of Genetics, Monash Health, Melbourne, Australia.
  • Pantaleoni C; Department of Paediatrics, Monash University, Melbourne, Australia.
  • Roche E; Pediatric Highly Intensive Care Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
  • Sherlock M; Developmental Neurology Unit, Fondazione IRCCS Istituto Neurologico C. Besta, Milan, Italy.
  • Springer A; Department of Paediatric Growth, Diabetes and Endocrinology, Tallaght University Hospital, Dublin, Ireland.
  • White SM; Department of Endocrinology and Diabetes Mellitus, Tallaght University Hospital, Dublin, Ireland.
  • Tatton-Brown K; Department of Endocrinology, Beaumont Hospital, Dublin, Ireland.
Am J Med Genet A ; 179(4): 588-594, 2019 04.
Article em En | MEDLINE | ID: mdl-30793471
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Anormalidades Múltiplas / Deformidades Congênitas da Mão / Anormalidades Craniofaciais / Hipotireoidismo Congênito / Complexo Repressor Polycomb 2 / Dedos / Proteína Potenciadora do Homólogo 2 de Zeste / Transtornos do Crescimento / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Degeneração Retiniana / Anormalidades Múltiplas / Deformidades Congênitas da Mão / Anormalidades Craniofaciais / Hipotireoidismo Congênito / Complexo Repressor Polycomb 2 / Dedos / Proteína Potenciadora do Homólogo 2 de Zeste / Transtornos do Crescimento / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido