Literature DB >> 32718497

Optimizing Genetic Diagnosis of Neurodevelopmental Disorders in the Clinical Setting.

David Joshua Michelson1, Robin Dawn Clark2.   

Abstract

Progress in medical genetics has changed the practice of medicine in general and child neurology in particular. A genetic diagnosis has become critically important in determining optimal management of many neurodevelopmental disorders, making genetic testing a routine consideration of patient care in outpatient and inpatient settings. Today's child neurologists should be familiar with various genetic testing modalities and their appropriate use. Molecular genetic testing of children with unexplained developmental delays and/or congenital anomalies has a 20% to 30% chance of identifying a causative etiology. Newer methods have made genetic testing more widely available and sensitive but also more likely to produce ambiguous results.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Autism spectrum disorder, ASD; Genetic testing; Global developmental delay, GDD; Intellectual disability, ID; Multiple congenital anomalies, MCA; Neurodevelopmental disabilities, NDD; Whole exome sequencing, WES; Whole genome sequencing, WGS

Mesh:

Year:  2020        PMID: 32718497     DOI: 10.1016/j.cll.2020.05.001

Source DB:  PubMed          Journal:  Clin Lab Med        ISSN: 0272-2712            Impact factor:   1.935


  4 in total

1.  A comprehensive WGS-based pipeline for the identification of new candidate genes in inherited retinal dystrophies.

Authors:  María González-Del Pozo; Elena Fernández-Suárez; Nereida Bravo-Gil; Cristina Méndez-Vidal; Marta Martín-Sánchez; Enrique Rodríguez-de la Rúa; Manuel Ramos-Jiménez; María José Morillo-Sánchez; Salud Borrego; Guillermo Antiñolo
Journal:  NPJ Genom Med       Date:  2022-03-04       Impact factor: 8.617

2.  Identification of a novel nonsense homozygous mutation of LINS1 gene in two sisters with intellectual disability, schizophrenia, and anxiety.

Authors:  Chia-Hsiang Chen; Yu-Shu Huang; Ting-Hsuan Fang
Journal:  Biomed J       Date:  2021-08-24       Impact factor: 4.910

3.  Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease.

Authors:  Marisol Delea; Lucia S Massara; Lucia D Espeche; María Paz Bidondo; Pablo Barbero; Jaen Oliveri; Paloma Brun; Mónica Fabro; Micaela Galain; Cecilia S Fernández; Melisa Taboas; Carlos D Bruque; Jorge E Kolomenski; Agustín Izquierdo; Ariel Berenstein; Viviana Cosentino; Celeste Martinoli; Mariana Vilas; Mónica Rittler; Rodrigo Mendez; Lilian Furforo; Rosa Liascovich; Boris Groisman; Sandra Rozental; Liliana Dain
Journal:  Genes (Basel)       Date:  2022-06-29       Impact factor: 4.141

4.  Craniofacial features of 3q29 deletion syndrome: Application of next-generation phenotyping technology.

Authors:  Bryan C Mak; Rossana Sanchez Russo; Michael J Gambello; Nicole Fleischer; Emily D Black; Elizabeth Leslie; Melissa M Murphy; Jennifer Gladys Mulle
Journal:  Am J Med Genet A       Date:  2021-05-03       Impact factor: 2.802

  4 in total

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