Literature DB >> 31501260

Genetic Counseling in Neurodevelopmental Disorders.

Alyssa Blesson1, Julie S Cohen2,3.   

Abstract

Neurodevelopmental disorders (NDDs), including global developmental delay (GDD), intellectual disability (ID), and autism spectrum disorder (ASD), represent a continuum of developmental brain dysfunction. Although the etiology of NDD is heterogeneous, genetic variation represents the largest contribution, strongly supporting the recommendation for genetic evaluation in individuals with GDD/ID and ASD. Technological advances now allow for a specific genetic diagnosis to be identified in a substantial portion of affected individuals. This information has important ramifications for treatment, prognosis, and recurrence risk, as well as psychological and social benefits for the family. Genetic counseling is a vital service to enable patients and their families to understand and adapt to the genetic contribution to NDDs. As the demand for genetic evaluation for NDDs increases, genetic counselors will have a predominant role in the ongoing evaluation of NDDs, especially as identification of genetic etiologies has the potential to lead to targeted treatments for NDDs in the future.
Copyright © 2020 Cold Spring Harbor Laboratory Press; all rights reserved.

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Year:  2020        PMID: 31501260      PMCID: PMC7117955          DOI: 10.1101/cshperspect.a036533

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Med        ISSN: 2157-1422            Impact factor:   6.915


  58 in total

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3.  Receiving the initial Down syndrome diagnosis: a comparison of prenatal and postnatal parent group experiences.

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Journal:  Intellect Dev Disabil       Date:  2013-12

4.  'Why us?' Causal attributions of childhood cancer survivors, survivors' parents and community comparisons - a mixed methods analysis.

Authors:  J Vetsch; C E Wakefield; E L Doolan; C Signorelli; B M McGill; L Moore; P Techakesari; R Pieters; A F Patenaude; M McCarthy; R J Cohn
Journal:  Acta Oncol       Date:  2019-01-06       Impact factor: 4.089

5.  Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions.

Authors:  Anne C Madeo; Kathleen E O'Brien; Barbara A Bernhardt; Barbara B Biesecker
Journal:  Am J Med Genet A       Date:  2012-06-18       Impact factor: 2.802

6.  Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study.

Authors:  Sally Ozonoff; Gregory S Young; Alice Carter; Daniel Messinger; Nurit Yirmiya; Lonnie Zwaigenbaum; Susan Bryson; Leslie J Carver; John N Constantino; Karen Dobkins; Ted Hutman; Jana M Iverson; Rebecca Landa; Sally J Rogers; Marian Sigman; Wendy L Stone
Journal:  Pediatrics       Date:  2011-08-15       Impact factor: 7.124

7.  Utility of Whole Exome Sequencing for Genetic Diagnosis of Previously Undiagnosed Pediatric Neurology Patients.

Authors:  Maya Kuperberg; Dorit Lev; Lubov Blumkin; Ayelet Zerem; Mira Ginsberg; Ilan Linder; Nirit Carmi; Sarah Kivity; Tally Lerman-Sagie; Esther Leshinsky-Silver
Journal:  J Child Neurol       Date:  2016-08-29       Impact factor: 1.987

Review 8.  The metabolic evaluation of the child with an intellectual developmental disorder: diagnostic algorithm for identification of treatable causes and new digital resource.

Authors:  Clara D M van Karnebeek; Michael Shevell; Johannes Zschocke; John B Moeschler; Sylvia Stockler
Journal:  Mol Genet Metab       Date:  2014-01-24       Impact factor: 4.797

9.  Predictors of psychological morbidity in parents of children with intellectual disabilities.

Authors:  Stephen Gallagher; Anna C Phillips; Christopher Oliver; Douglas Carroll
Journal:  J Pediatr Psychol       Date:  2008-04-22

10.  Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.

Authors:  Michelle M Clark; Zornitza Stark; Lauge Farnaes; Tiong Y Tan; Susan M White; David Dimmock; Stephen F Kingsmore
Journal:  NPJ Genom Med       Date:  2018-07-09       Impact factor: 8.617

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  6 in total

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Journal:  Am J Transl Res       Date:  2022-08-15       Impact factor: 3.940

2.  Multidisciplinary Consulting Team for Complicated Cases of Neurodevelopmental and Neurobehavioral Disorders: Assessing the Opportunities and Challenges of Integrating Pharmacogenomics into a Team Setting.

Authors:  Pritmohinder S Gill; Amanda L Elchynski; Patricia A Porter-Gill; Bradley G Goodson; Mary Ann Scott; Damon Lipinski; Amy Seay; Christina Kehn; Tonya Balmakund; G Bradley Schaefer
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Review 3.  Genetic Counseling and the Central Tenets of Practice.

Authors:  Barbara Biesecker
Journal:  Cold Spring Harb Perspect Med       Date:  2020-03-02       Impact factor: 6.915

Review 4.  The development of the social brain in baby siblings of children with autism.

Authors:  Douglas C Dean; Abigail Freeman; Janet Lainhart
Journal:  Curr Opin Psychiatry       Date:  2020-03       Impact factor: 4.787

Review 5.  Diagnostic Utility of Genome-Wide DNA Methylation Analysis in Mendelian Neurodevelopmental Disorders.

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Journal:  Int J Mol Sci       Date:  2020-12-06       Impact factor: 5.923

Review 6.  Best Practices in Structural Neuroimaging of Neurodevelopmental Disorders.

Authors:  Lea L Backhausen; Megan M Herting; Christian K Tamnes; Nora C Vetter
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  6 in total

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