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Parental age effects and Rett syndrome.
Fang, Xiaolan; Baggett, Lauren M; Caylor, Raymond C; Percy, Alan K; Neul, Jeffrey L; Lane, Jane B; Glaze, Daniel G; Benke, Tim A; Marsh, Eric D; Motil, Kathleen J; Barrish, Judy O; Annese, Fran E; Skinner, Steven A.
Afiliação
  • Fang X; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Baggett LM; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Caylor RC; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Percy AK; The University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Neul JL; Vanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Lane JB; The University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Glaze DG; Baylor College of Medicine, Houston, Texas, USA.
  • Benke TA; University of Colorado School of Medicine, Children's Hospital Colorado-Aurora, Denver, Colorado, USA.
  • Marsh ED; Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Motil KJ; Vanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Barrish JO; Baylor College of Medicine, Houston, Texas, USA.
  • Annese FE; Greenwood Genetic Center, Greenwood, South Carolina, USA.
  • Skinner SA; Greenwood Genetic Center, Greenwood, South Carolina, USA.
Am J Med Genet A ; 194(2): 160-173, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37768187
Rett syndrome (RTT) is a progressive neurodevelopmental disorder, and pathogenic Methyl-CpG-binding Protein 2 (MECP2) variants are identified in >95% of individuals with typical RTT. Most of RTT-causing variants in MECP2 are de novo and usually on the paternally inherited X chromosome. While paternal age has been reported to be associated with increased risk of genetic disorders, it is unknown whether parental age contributes to the risk of the development of RTT. Clinical data including parental age, RTT diagnostic status, and clinical severity are collected from 1226 participants with RTT and confirmed MECP2 variants. Statistical analyses are performed using Student t-test, single factor analysis of variance (ANOVA), and multi-factor regression. No significant difference is observed in parental ages of RTT probands compared to that of the general population. A small increase in parental ages is observed in participants with missense variants compared to those with nonsense variants. When we evaluate the association between clinical severity and parental ages by multiple regression analysis, there is no clear association between clinical severity and parental ages. Advanced parental ages do not appear to be a risk factor for RTT, and do not contribute to the clinical severity in individuals with RTT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Rett Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Rett Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article