Literature DB >> 25350348

Evaluation of the Affymetrix CytoScan(®) Dx Assay for developmental delay.

Bryn D Webb1, Rebecca J Scharf, Emily A Spear, Lisa J Edelmann, Annemarie Stroustrup.   

Abstract

The goal of molecular cytogenetic testing for children presenting with developmental delay (DD) is to identify or exclude genetic abnormalities that are associated with cognitive, behavioral and/or motor symptoms. Until 2010, chromosome analysis was the standard first-line genetic screening test for evaluation of patients with DD when a specific syndrome was not suspected. In 2010, The American College of Medical Genetics and several other groups recommended chromosomal microarray as the first-line test in children with DDs, multiple congenital anomalies and/or autism. This test is able to detect regions of genomic imbalances at a much finer resolution than G-banded karyotyping. Until recently, no chromosomal microarray testing had been approved by the US FDA. This article focuses on the use of the Affymetrix CytoScan(®) Dx Assay (Santa Clara, CA, USA), the first chromosomal microarray to receive FDA approval for the genetic evaluation of individuals with DD.

Entities:  

Keywords:  Affymetrix CytoScan® Dx Assay; chromosomal microarray; genetic testing; global developmental delay; mental retardation

Mesh:

Year:  2014        PMID: 25350348      PMCID: PMC4415685          DOI: 10.1586/14737159.2015.975213

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  15 in total

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Authors:  Eric M Morrow
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2010-11       Impact factor: 8.829

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Review 3.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

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Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

Review 4.  Pathogenic or not? Assessing the clinical relevance of copy number variants.

Authors:  J Y Hehir-Kwa; R Pfundt; J A Veltman; N de Leeuw
Journal:  Clin Genet       Date:  2013-08-21       Impact factor: 4.438

5.  Origins and functional impact of copy number variation in the human genome.

Authors:  Donald F Conrad; Dalila Pinto; Richard Redon; Lars Feuk; Omer Gokcumen; Yujun Zhang; Jan Aerts; T Daniel Andrews; Chris Barnes; Peter Campbell; Tomas Fitzgerald; Min Hu; Chun Hwa Ihm; Kati Kristiansson; Daniel G Macarthur; Jeffrey R Macdonald; Ifejinelo Onyiah; Andy Wing Chun Pang; Sam Robson; Kathy Stirrups; Armand Valsesia; Klaudia Walter; John Wei; Chris Tyler-Smith; Nigel P Carter; Charles Lee; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2009-10-07       Impact factor: 49.962

6.  CAT/CLAMS. A tool for the pediatric evaluation of infants and young children with developmental delay. Clinical Adaptive Test/Clinical Linguistic and Auditory Milestone Scale.

Authors:  R C Wachtel; B K Shapiro; F B Palmer; M C Allen; A J Capute
Journal:  Clin Pediatr (Phila)       Date:  1994-07       Impact factor: 1.168

7.  Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories.

Authors:  Karen D Tsuchiya; Lisa G Shaffer; Swaroop Aradhya; Julie M Gastier-Foster; Ankita Patel; M Katharine Rudd; Julie Sanford Biggerstaff; Warren G Sanger; Stuart Schwartz; James H Tepperberg; Erik C Thorland; Beth A Torchia; Arthur R Brothman
Journal:  Genet Med       Date:  2009-12       Impact factor: 8.822

8.  ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.

Authors:  Sarah T South; Charles Lee; Allen N Lamb; Anne W Higgins; Hutton M Kearney
Journal:  Genet Med       Date:  2013-09-26       Impact factor: 8.822

9.  Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.

Authors:  Stuart A Scott; Ninette Cohen; Tracy Brandt; Gokce Toruner; Robert J Desnick; Lisa Edelmann
Journal:  Genet Med       Date:  2010-02       Impact factor: 8.822

10.  Clinical genetic testing for patients with autism spectrum disorders.

Authors:  Yiping Shen; Kira A Dies; Ingrid A Holm; Carolyn Bridgemohan; Magdi M Sobeih; Elizabeth B Caronna; Karen J Miller; Jean A Frazier; Iris Silverstein; Jonathan Picker; Laura Weissman; Peter Raffalli; Shafali Jeste; Laurie A Demmer; Heather K Peters; Stephanie J Brewster; Sara J Kowalczyk; Beth Rosen-Sheidley; Caroline McGowan; Andrew W Duda; Sharyn A Lincoln; Kathryn R Lowe; Alison Schonwald; Michael Robbins; Fuki Hisama; Robert Wolff; Ronald Becker; Ramzi Nasir; David K Urion; Jeff M Milunsky; Leonard Rappaport; James F Gusella; Christopher A Walsh; Bai-Lin Wu; David T Miller
Journal:  Pediatrics       Date:  2010-03-15       Impact factor: 7.124

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1.  An ethical analysis of divergent clinical approaches to the application of genetic testing for autism and schizophrenia.

Authors:  E Morris; M O'Donovan; A Virani; J Austin
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2.  Complex Chromosomal Rearrangements in B-Cell Lymphoma: Evidence of Chromoanagenesis? A Case Report.

Authors:  Veronica Ortega; Alka Chaubey; Christina Mendiola; William Ehman; Kumari Vadlamudi; Barbara Dupont; Gopalrao Velagaleti
Journal:  Neoplasia       Date:  2016-04       Impact factor: 5.715

3.  Translational Medicine in Neurological Disorders: A Genomic Perspective.

Authors:  Giulia Gentile; Sebastiano Cavallaro
Journal:  Curr Genomics       Date:  2019-04       Impact factor: 2.236

4.  Double aneuploidy mosaicism involving chromosomes 18 and 21 in a neonate.

Authors:  Christina Mendiola; Veronica Ortega; Allison Britt; Rafael Fonseca; Gopalrao Velagaleti
Journal:  Mol Cytogenet       Date:  2022-01-24       Impact factor: 2.009

5.  Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias.

Authors:  Hao-Ling Cheng; Ya-Ru Shao; Yi Dong; Hai-Lin Dong; Lu Yang; Yin Ma; Ying Shen; Zhi-Ying Wu
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